US 6,595,992 B1Grant
Method and apparatus for spinal fixation
Issue Date:2003-07-22
•236 Claims
•12 Drawing Sheets
Abstract
A spinal fixation implant system for correction and fixation of the human spine to facilitate an anatomically correct fusion. The spinal fixation system may include a connector, a spinal rod, a spinal fixation component, a sleeve, and a fastener. The spinal fixation component preferably includes a fixation device such as a hook or screw for securing the spinal rod to vertebrae of the thoracic or lumbar spine. The spinal fixation component preferably includes a threaded end on its top that is adapted to receive the fastener. The fixation component may include a body having a tapered cavity for engaging the receiving end of the connector. Tightening of the fastener preferably downwardly translates the sleeve over the fixation component body to force the connector through the tapered cavity, which compresses the receiving end about the spinal rod to fixably connect the spinal rod and the spinal fixation component. In an alternate embodiment, assembly pliers may be used to move the connector into the tapered cavity. The fixation component may also include a rotatable fixation member.
Metadata
Assignee
- Spinal Concepts, Inc.
Inventors
- Erik J. Wagner
- Vincent J. Jannetty
Application Information
Application Number:US 08/942,325
Filing Date:1997-10-01
Priority Date:1996-10-24
Art Unit:7
Classifications
IPC:
A61B 1756
Field of Search:
606 53606 61606 72606 73623 1711
Patent Drawings (12 sheets)
Description
PRIOR APPLICATION
[0002] This application is a continuation-in-part of U.S. patent application Ser. No. 08/740,123 filed on Oct. 24, 1996.
BACKGROUND OF THE INVENTION
[0003] 1. Field of the Invention
[0004] The present invention generally relates to spinal fixation systems and the like. More particularly, an embodiment of the invention relates to a spinal implant system for correction, fixation, and stabilization of the human spine to allow the development of a solid spinal fusion.
[0005] 2. Description of the Related Art
[0006] Spinal fixation, such as lumbar sacral fusion and the correction of spinal deformities such as scoliotic curves, is a well known and frequently used medical procedure. Pedicle, lateral, and oblique mounting devices may be used to secure corrective spinal instrumentation to a portion of the spine that has been selected to be fused by arthrodesis.
[0007] A spinal fixation system typically includes corrective spinal instrumentation that is attached to selected vertebrae of the spine by screws, hooks, and clamps. The corrective spinal instrumentation includes spinal rods or plates that are generally parallel to the patient's back. The corrective spinal instrumentation may also include transverse connecting rods that extend between neighboring spinal rods. Spinal fixation systems are used to correct problems in the lumbar and thoracic portions of the spine, and are often installed posterior to the spine on opposite sides of the spinous process and adjacent to the transverse process.
[0008] Various types of screws, hooks, and clamps have been used for attaching corrective spinal instrumentation to selected portions of the patient's spine. Examples of pedicle screws and other types of attachments are illustrated in U.S. Pat. Nos. 4,763,644; 4,805,602; 4,887,596; 4,950,269; and 5,129,388. Each of these patents is incorporated by reference as if fully set forth herein.
[0009] An eyebolt assembly of the TSRH® spinal system sold by Danek Medical Inc. is illustrated in FIG. 1. The eyebolt assembly 2 encircles spinal rod 4 such that assembly mass completely surrounds the spinal rod. The spinal rod must be inserted through the eyebolt, which rests within the yoke of spinal hook 8. The spinal hook attaches the spinal rod to a bony element of the spine. A nut 6 is threaded onto a post of the eyebolt assembly to fixably secure the rod within the yoke. The nut is tightened so that the assembly resists axial, torsional, and shear forces to inhibit motion of the spinal rod relative to the assembly in the directions indicated by the arrows in FIG. 1. Further details of the TSRH® spinal system are provided in the TSRH® Spinal Implant System Surgical Technique Manual and the TSRH® Crosslink Surgical Technique Manual. Both of these publications are available from Danek Medical Inc. and are incorporated by reference as if fully set forth herein.
[0010] Manual insertion of a spinal rod through the bores of a number of spaced-apart eyebolts within a surgical wound tends to be difficult. The bore axis of each eyebolt must be properly aligned along a common axis, which is difficult since the corrective procedure requires that the spinal rod initially be placed under stress to resist deforming forces of the spine. Therefore, the use of systems such as the TSRH® spinal system may require that a predetermined number of screws or hooks be pre-loaded onto the spinal rod in a particular order and spacing prior to the insertion of the spinal rod into the surgical wound. After insertion of the spinal system into the surgical wound, however, it is often necessary to add, delete, or reposition one or more hooks or screws. Before such modifications can be made, the spinal system typically must be removed from the surgical wound and at least partially disassembled.
[0011] To overcome such problems, some spinal fixation systems include “open back” hooks or screws to allow a spinal rod to be dropped into the open back of the hook or screw and secured within the open back by a separate component and a set screw. Such a system is illustrated in U.S. Pat. No. 5,102,412 to Rogozinski, which is incorporated by reference as if fully set forth herein. Such systems tend to be susceptible to fatigue stress failure and require assembly within the surgical wound. In addition, adding a hook or screw to the construct tends to require that the spinal rod first be repositioned. A further disadvantage of this approach is that component mass completely surrounds the spinal rod, resulting in an increase in the profile width of the device and greater impingement of the device upon the fusion mass. A low profile width is generally desired to minimize sinus formation and soft tissue irritation from hardware prominence.
[0012] U.S. Pat. No. 5,242,445 to Ashman relates to a “split eyebolt” assembly for adding eyebolts to an assembled spinal fixation construction. Attaching the split eyebolt to a spinal rod requires a special crimping tool to crimp the split eyebolt over the rod. The crimping tool tends to be difficult to operate within the surgical wound. Furthermore, the threads of the opposing sides of the split eyebolt are often misaligned after crimping, making it difficult or impossible to thread a nut onto the split eyebolt. The split eyebolt also completely encircles the spinal rod thereby increasing the impingement of the construct upon the fusion mass.
[0013] It is therefore desirable that an improved spinal fixation system be derived that facilitates assembly and surgical implantation by allowing the spinal rod to be positioned within the surgical wound (a) after the fixation components (e.g., screws, hooks) have been implanted, (b) without modifying the fixation components, and (c) whereby fixation components may be subsequently added, deleted, and/or repositioned without disassembling the system.
SUMMARY OF THE INVENTION
[0014] In accordance with the present invention, a spinal fixation system is provided that largely eliminates or reduces the aforementioned disadvantages of conventional spinal fixation constructions. An embodiment of the invention relates to an implant system for fixation of the human spine that includes a spinal rod, a fixation component, a connector, and a fastener.
[0015] The connector may be used to connect the spinal rod to the fixation component and preferably includes a receiving end and a fastening end. The receiving end may contain a first arm and a second arm that together form a substantially U-shaped borehole into which the spinal rod may be axially positioned. The receiving end preferably surrounds only part of the spinal rod such that the unsurrounded portion of the spinal rod is exposed from the borehole. The exposed portion of the spinal rod may extend out of an open end of the U-shaped borehole. The spinal rod may be circular and preferably includes a cross-section having a circumferential portion. The receiving end of the connector preferably surrounds and engages greater than about π radians and less than about 2π radians of the circumferential portion.
[0016] The receiving end of the connector preferably acts as a “pinch clamp” by exerting a clamping force on opposing sides of the spinal rod to secure the spinal rod within the borehole. The connector preferably contains a slot between the receiving end and the fastening end that enables the first arm and the second arm to be deflected relative to one another. The deflection of the arms allows the distance between a tip of the first arm and a tip of the second arm to be changed so that the spinal rod may be inserted through an open end of the U-shaped borehole that is defined between the tips of the arms.
[0017] The fixation component preferably includes a fixation device such as a bone screw or hook for engaging vertebrae of the thoracic or lumbar spine. The fixation component also preferably includes a body containing a cavity with an inner surface. The cavity is preferably sized to receive a portion of the connector. The connector is preferably partially disposed within the cavity such that at least a portion of the fastening end extends from the cavity, whereby the inner surface of the cavity engages an outer surface of the receiving end. The cavity of the body is preferably a tapered cavity that narrows in a direction from a first end of the cavity to a second end of the cavity. The tapered cavity preferably surrounds a portion of the receiving end and imparts a compressive force against the receiving end to secure the spinal rod within the borehole.
[0018] The fastener preferably engages both the body and the portion of the fastening end that extends from the cavity. The fastener may secure the connector and the fixation component together. The fastener is preferably a nut adapted to be threaded upon the fastening end. The fastener may be selectively tightened to allow an engagement between the connector and the spinal rod that may be overcome by the application of a distraction force to the connector. Rotation of the nut in a tightening direction about the fastening end preferably draws a portion of the receiving end through the tapered cavity, causing the inner surface of the cavity to compress the arms of the receiving end. In turn, the arms may exert a compressive force against the spinal rod to clamp it within the borehole. The magnitude of the compressive force against the spinal rod preferably varies as a function of the degree to which the nut is tightened. The open end of the U-shaped borehole preferably has a width that can be adjusted by tightening the fastener.
[0019] The fixation component may include a spacer located between the fastener and the spinal rod for laterally offsetting the fixation device a selected lateral distance from the spinal rod. The spacer may include a surface having a plurality of radially-spaced teeth. The fixation component may comprise a plurality of radially-spaced protrusions adapted to fit adjacent to the teeth on the surface of the spacer. The tightening of the nut preferably causes the spacer and the fixation component to become pressed together such that a complementary engagement between the teeth of the spacer and the protrusions of the fixation device is formed to inhibit rotation of the fixation device about the spacer.
[0020] The body may include a U-shaped yoke formed between a top section and a bottom section that each have an edge adjacent to the yoke. The tapered cavity preferably is formed between the top section and the bottom section and extends in a perpendicular direction relative to the U-shaped yoke. The fixation component is preferably adapted to pivot about the spinal rod in a substantially vertical plane. The edges of the top and bottom sections preferably contact the spinal rod during the pivoting of the fixation component to define the range of pivotal motion of the fixation component about the spinal rod. The edges are preferably curved in a direction away from the spinal rod to increase the range of pivotal motion of the fixation component.
[0021] The fixation component may include a transverse connector to maintain a fixed distance between the spinal rod and a neighboring spinal rod. The transverse connector may include a reduced section that has a width less than that of the body, allowing the reduced section to be more easily bent. The reduced section may be bent to shorten the lateral distance between the spinal rod and an adjacent spinal rod. The transverse connector may contain a beveled section between the body and the reduced section.
[0022] In an embodiment, the connector includes a receiving end forming a substantially U-shaped borehole and a capped end opposite the receiving end. The connector may be forced into the cavity of a fixation component body with an instrument such as a pair of assembly pliers. The instrument preferably includes a first elongated member and a second elongated member. The elongated members may be moved relative to one another to exert a compressive force against the connector and the fixation component to move the connector within the cavity of the fixation component body. The first elongated member preferably includes a curvate indention for engaging the spinal rod. The second elongated member preferably includes a borehole for receiving an end of the connector.
[0023] In an embodiment, the fixation component includes a fastening end. The fastening end preferably is adapted to receive a fastener (e.g., threaded nut). Downward translation of the fastener preferably moves a sleeve downwardly over the body of the fixation component. The sleeve preferably contains a substantially U-shaped opening having a angled locking surface for engaging the spinal rod. During assembly, the fastener is preferably tightened to move the sleeve downwardly, thereby imparting a force on the spinal rod that causes the connector to move through the tapered cavity.
[0024] In an embodiment, the fixation component may include a pivotable fixation device. The fixation device is preferably adapted to pivot about the body of the fixation component along the longitudinal axis of the body. The body of the fixation component may be adapted to inhibit the lateral motion of the fixation device. The body of the fixation component may be adapted to engage a portion of the connector.
[0025] In an embodiment the connector may include an opening adapted to completely surround the circumferential portion of the spinal rod. The connector may include a slot running through the center of the connector, communicating with the opening. The slot may be adapted to allow the circumference of the opening to vary. Insertion of a spinal rod preferably causes the slot to widen such that the circumference of the opening increases. The connector may be placed within the fixation component such that the slot is narrowed to secure a spinal rod to the connector.
[0026] An advantage of the present invention relates to a fixation component that may be added to or deleted from a spinal fixation construct in a surgical wound without disassembling the construct.
[0027] Another advantage of the present invention relates to a spinal fixation system requiring minimal assembly within the surgical wound.
[0028] Yet another advantage of the present invention relates to a spinal fixation system having a relatively narrow profile width to reduce impingement upon the fusion mass.
BRIEF DESCRIPTION OF THE DRAWINGS
[0029] Further advantages of the present invention will become apparent to those skilled in the art with the benefit of the following detailed description of the preferred embodiments and upon reference to the accompanying drawings in which:
[0030] FIG. 1 depicts a TSRH® spinal system eyebolt assembly;
[0031] FIG. 2 depicts a side view of an embodiment of a spinal fixation system connected to a vertebra;
[0032] FIG. 3 depicts a top view of the spinal fixation system of FIG. 1;
[0033] FIG. 4 depicts a side view of a tapered connector constructed in accordance with the present invention;
[0034] FIG. 5 depicts a side view of a tapered connector prior to assembly with a fixation component body and a spinal rod;
[0035] FIG. 6 depicts a side view of a tapered connector assembled with a spinal fixation component and a spinal rod;
[0036] FIG. 7 depicts a side view of a transverse connector disposed between a pair of spinal rods in accordance with the present invention;
[0037] FIG. 8 depicts a front view and side view partially in section of a bone screw constructed according to teachings of the present invention;
[0038] FIG. 9 depicts a front view and side view partially in section of a bone screw having radially-spaced protrusions in accordance with the present invention;
[0039] FIG. 10 depicts a front view and a side view partially in section of a reversible fixation component constructed according to teachings or the present invention;
[0040] FIG. 11 depicts a side view partially in section of a spacer disposed between a spinal rod and a fastener in accordance with the present invention;
[0041] FIG. 12 depicts a side view partially in section of a spinal fixation system prior to assembly;
[0042] FIG. 13 depicts a side view partially in section of a spinal fixation system assembled with an instrument;
[0043] FIG. 14 depicts a side view partially in section of a spinal fixation system that includes a set screw engaging a connector;
[0044] FIG. 15 depicts a spinal fixation system that includes a locking sleeve;
[0045] FIG. 16 depicts a side view of the spinal fixation system of FIG. 15 after assembly;
[0046] FIG. 17 depicts a side view partially in section of the system of FIG. 15 after assembly;
[0047] FIG. 18 depicts a side view of a spinal fixation system that includes a rotatable fixation device;
[0048] FIG. 19 depicts a top view of a fixation component that includes a rotatable fixation device;
[0049] FIG. 20 depicts a cross sectional view of the side of a spinal fixation system that includes a rotatable fixation device;
[0050] FIG. 21 depicts a side view of a tapered connector adapted to completely surround a portion of a spinal rod;
[0051] FIG. 22 depicts a cross sectional view of the side of a spinal fixation system that includes a rotatable fixation device and a connector adapted to completely surround a portion of a spinal rod;
[0052] FIG. 23 depicts a rear view of a spinal fixation system adapted to completely surround a portion of a spinal rod; and
[0053] FIG. 24 depicts a cross sectional view of the side of a spinal fixation system adapted to completely surround a portion of a spinal rod.
[0054] While the invention is susceptible to various modifications and alternative forms, specific embodiments thereof are shown by way of example in the drawings and will herein be described in detail. It should be understood, however, that the drawings and detailed description thereto are not intended to limit the invention to the particular form disclosed, but on the contrary, the intention is to cover all modifications, equivalents and alternatives falling within the spirit and scope of the present invention as defined by the appended claims.
DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS
[0055] FIG. 2 depicts a spinal fixation system 10 constructed according to teachings of the present invention. In an embodiment of the invention, spinal fixation system 10 includes a spinal rod 12 generally aligned parallel with a portion of the spine. Connector 16 secures spinal fixation components to the spinal rod via fastener 18. The fixation components may include various fixation devices including bone screw 14, transverse connector 20, and spinal hooks 22 and 24.
[0056] Spinal rod 12 is preferably constructed of stainless steel or another relatively rigid material. The spinal rod preferably has a substantially circular cross-section (although other cross-sectional geometries may be employed) and a diameter between about ⅛ of an inch and about ¼ of an inch. The spinal rod may have a shot-peened surface to increase its resistance to fatigue failure. The spinal rod may impart forces against the spine to maintain a portion of the spine in a fixed position to correct a spinal deformity or injury. The spinal rod may be contoured to a selected shape prior to or after surgical implantation.
[0057] Bone screw 14 is preferably inserted within the main body of a vertebra 26 and may contain threads 28 to create a fixable engagement with the vertebra. Alternatively, the bone screw may have a substantially smooth shank containing no threading. The stress imparted to spinal fixation systems resulting from a spinal deformity may cause fatigue failure of a threaded bone screw if a solid spinal fusion does not develop after a period of time. Threaded screws having relatively long shanks tend to fail at a location adjacent to the screw head. A substantially smooth, unthreaded shank tends to remove the stress concentration on the screw shank from a location adjacent to the screw head where failure of the screw often occurs. The bone screw may also include a tap relief 30 to facilitate its insertion into vertebra 26. The angle of the bone screw relative to the spinal rod is preferably adjustable. The bone screw may be angled to correct the angle 32 of a vertebra relative to other vertebrae in the spine. The angle between the bone screw and spinal rod is preferably fixable by tightening fastener 18. Furthermore, the height of the vertebra 26 may be adjusted by applying a distraction force in the directions indicated by arrow 34 between a pair of fixation devices such as bone screw 14 and spinal hook 24 prior to tightening fasteners 18. The distraction force may be applied with the use of a tool in a manner well known to those skilled in the art.
[0058] The spinal hooks 22 and 24 may be any of a number of types of hooks well known to those skilled in the art including large laminar, small laminar, thoracic laminar, and pedicle hooks. Each spinal hook may be positioned in the caudal direction (illustrated by hook 24 in FIG. 2) or in the cranial direction (illustrated by hook 22 in FIG. 2). Spinal hooks may be positioned on opposing sides of the spinal rod as shown in FIG. 2.
[0059] FIG. 3 depicts a top view of an embodiment of spinal fixation system 10 that includes a pair of spinal rods 12 in spaced relation on each side of the vertical axis 40 of the spine. Spinal hooks 22 and 24 are preferably positioned for attachment to bony elements of the posterior human spine. One or more transverse connectors 20 may be used to rigidly link the rods to improve the strength of the assembly. Each of the fixation components may be attached to the spinal rod using a fastener 18 that engages connector 16 and the fixation component.
[0060] Transverse connector 20 may connect neighboring rods to increase the rigidity of the construct and to prevent the movement of the rods relative to one another. The transverse connector may be attached to the spinal rod using crosslinking plates that are well known to those skilled in the art and described in the TSRH® Crosslink Surgical Technique Manual, which is incorporated by reference herein. It is preferred that neighboring rods be connected by two transverse connectors that may be aligned parallel and in spaced relation from one another. If the spinal rod is bent, transverse connector 20 is preferably attached to the spinal rod at a location other than the “peak” of the curved section of the rod so that additional stress is not placed at that location.
[0061] An embodiment of connector 16 is illustrated in FIG. 4. The connector preferably includes a fastening end 50 and a receiving end 54 opposite the fastening end. The fastening end may be a threaded end containing male machine threads 52 that are adapted to engage a fastener. The fastener is preferably a nut. The receiving end preferably includes a first arm 56 and a second arm 58 that together form a U-shaped borehole 62. The first arm has a tip 72 and the second arm has a tip 74 (each labeled in FIG. 5), and an opening 60 or open end is preferably defined by the tips of the first and second arm. A slot 64 preferably extends between the receiving end and the fastening end. The slot may extend from borehole 62 proximate the receiving end to a location proximate the fastening end. The slot may terminate in an enlarged opening 66 within the receiving end. The borehole is preferably adapted to receive a spinal rod 12 such that the first and second arms of the receiving end surround more than about half of a circumferential portion of the spinal rod.
[0062] The connector preferably does not completely surround the perimeter of the spinal rod. The unsurrounded portion of the spinal rod is preferably exposed from the open end 60 of the U-shaped borehole and may extend from the borehole through the open end. It is preferred that component mass be placed around only slightly greater than one-half of the circumference of the spinal rod to minimize the profile width of the construct. In this manner, the impingement of the construct upon the fusion mass is lessened, thereby reducing irritation of the surrounding tissue and facilitating the development of a correct spinal fusion in a minimal amount of time. Conventional assemblies tend to completely surround the spinal rod with component mass, causing a relatively greater impingement upon the fusion mass, which may interfere with fusion development.
[0063] The angle 68 in FIG. 4 is defined by the circumferential portion of a spinal rod that is surrounded by the first arm, second arm, and the end of slot 64. The angle 68 is preferably less than about 2π radians (e.g., 360° around the cross-section of the spinal rod) and greater than about π radians (e.g., 180° around the cross-section of the spinal rod). It is preferred that more than about half of the circumferential portion the spinal rod be surrounded by a portion of the receiving end (e.g., first arm, second arm end of slot 64) to allow the spinal rod to be adequately secured within the borehole. If less than half of the circumferential portion of the spinal rod were surrounded by the receiving end, forces resulting from spinal deformations might tend to pull the spinal rod from within borehole 62. First arm 58 and second arm 68 preferably engage the surface of greater than about half of the circumferential portion of the spinal rod.
[0064] The first arm and the second arm preferably each have an outside surface that is slightly tapered such that the distance between the outside surfaces of the arms narrows in a direction from tips 72 and 74 to the fastening end 50. The taper of the outside surfaces of the arms preferably defines a locking angle 70. Locking angle 70 is preferably a conical angle, although it may be formed within a substantially flat wedge instead. Locking angle 70 is preferably less than about 30°, more preferably less than about 25°, and more preferably still between about 1° and about 20°.
[0065] FIGS. 5 and 6 illustrate the insertion of spinal rod 12 within borehole 62 in an embodiment of the invention. The spinal rod is preferably axially positioned within the borehole by passing the spinal rod through opening 60. Slot 64 preferably enables deflection of the first arm and the second arm relative to one another to allow the width of opening 60 to be altered. In the absence of an external force of a selected magnitude against the first or second arms, the width of opening 60 is preferably less than the outside diameter 76 of the spinal rod. Receiving end 54 is preferably adapted to form a “snap-fit” engagement with the spinal rod that may be realized by forcing the spinal rod into the inner surfaces of tips 72 and 74 of the first and second arms, respectively. The force against the inner surfaces of the tips 72 and 74 preferably causes the arms to slightly deflect in opposite directions, resulting in a slight widening of at least a portion of the slot. In this manner, the width of opening 60 may be increased by an amount sufficient to allow the insertion of the spinal rod through opening 60 and into the borehole. Once the spinal rod is fully inserted within the borehole (as shown in FIG. 6), the arms preferably move back toward one another, causing the slot to narrow to its initial unstressed width. If the diameter of the spinal rod is slightly greater than that of the borehole, the arms may remain slightly deflected and the slot may remain slightly widened after the spinal rod is snapped into the borehole. It is generally preferred that the diameter of the spinal rod and the diameter of the borehole be equal.
[0066] In an embodiment of the invention, connector 16 connects the spinal rod to a fixation component that engages a portion of the spine. The fixation component preferably includes a fixation device such as a bone screw, hook, transverse connector, or similar device. The fixation component preferably includes a body 80 having a tapered cavity into which connector 16 may be inserted. The tapered cavity preferably tapers in a direction that is substantially perpendicular to the longitudinal axis of the fixation component. The tapered cavity preferably has a first end 84, a second end 86, and an inside surface 82. The inside surface 82 is preferably tapered at an angle that corresponds to locking angle 70. The tapered cavity preferably narrows in a direction from first end 84 to second end 86. The tapered cavity is preferably sized so that fastening end 50 and a portion of receiving end 54 may be inserted within the tapered cavity through an aperture proximate the first end. The outer width of the receiving end proximate tips 72 and 74 is preferably slightly greater than the width of the aperture proximate the first end, thereby inhibiting the complete insertion of the receiving end into the tapered cavity.
[0067] Fastener 18 may be a hex nut and preferably contains female threading 19, which is sized to fit the male machine threads of the fastening end 50. The nut preferably engages fastening end 50 and body 80 whereby rotating the fastener in a tightening direction creates a tensile force in the connector in direction 88. Tightening of the fastener preferably moves the connector within the tapered cavity in a direction from first end 84 to second end 86, thereby creating an interference fit between the arms of the receiving end and inside surface 82. As the fastener is tightened, the arms are preferably deflected toward one another such that the slot is narrowed and the arms of the receiving end exert a compressive force against the spinal rod disposed within the borehole.
[0068] The magnitude of the compressive force exerted by the receiving end on the spinal rod is preferably variable as a function of the degree to which the fastener is tightened. The fastener may be selectively tightened so that the connector is “loosely” engaged to the spinal rod. The “loose” engagement preferably fixes the position of the connector on the rod in the absence of a selected force against the connector, while allowing the connector to slide over the surface of the rod upon receiving a distraction force. For instance, the fastener may be partially tightened to loosely attach a connector and fixation device onto the rod at a selected location. A distraction force may be applied to the connector to move the connector to a selected location on the rod, and the fastener may then be fully tightened to maintain the connector at the selected location.
[0069] The arms 56 and 58 preferably exert a clamping force onto “opposite sides” of the rod (i.e., sections of the outer surface of the spinal rod that are separated by about 180°). The engagement between the arms 56 and 58 and the “opposite sides” of the spinal rod preferably “centers” the rod within the borehole as shown in FIG. 6 so that substantially no gaps exist between the inner surface of the arms and the spinal rod. The rod may be constrained on opposing sides in this manner to provide further resistance to forces that might otherwise result in axial movement of the rod. When the arms 56 and 58 are deflected to engage the spinal rod, the receiving end preferably forms a “locking taper” engagement with the spinal rod. A “locking taper” engagement is taken to mean a largely irreversible deflection of the receiving end. That is, if the fastener becomes loose after the receiving end has been compressed about the spinal rod, the clamping force exerted by the receiving end will be maintained to fixably hold the spinal rod within the borehole.
[0070] In an embodiment of the invention depicted in FIG. 7, a transverse connector 20 is disposed between a pair of spinal rods in spaced relation to secure the rods at a fixed distance 90. The spinal rods are fixed within the borehole of a connector in the manner depicted in FIGS. 5 and 6 and described above. The transverse connector may include a beveled surface between body 80 and a reduced section 92. Reduced section 92 preferably has a smaller width or diameter than body 80 to allow the reduced section to be bent more easily. Slight variations in distance 39 may be achieved by bending transverse connector 20 proximate reduced section 92. The bending of the transverse connector may be accomplished using a rod bender and a method well known to those skilled in the art. Alternately, the transverse connector may have a substantially constant width or diameter such that the width of section 92 and the width of body 80 are approximately equal.
[0071] The fixation component may include a bone screw that is used to correct the angle 32 between vertebrae. It is preferred that the bone screw be adapted to pivot about the spinal rod to form an oblique angle between the longitudinal axis of the spinal rod and the shank of the bone screw. The bone screw preferably can be pivoted in either direction 96 or direction 98 such that an oblique angle between about 90° and about 60° is formed between the shank and the longitudinal axis of the spinal rod. Other fixation devices (e.g., hooks) may be pivoted with respect the spinal rod in the same manner. As illustrated in FIG. 8, the tapered cavity may contain an engaging side 100 adapted to contact flat 102 of connector 16 to limit the pivoting of a fixation device (e.g., bone screw) about the spinal rod within a selected range, thereby preventing a gross misalignment that might complicate the assembly of the construct during a surgical procedure.
[0072] Body 80 preferably includes a top section 104 and a bottom section 106 that together form a U-shaped yoke 112 that is substantially perpendicular to inside surface 82 of the tapered cavity. The fixation component may pivot about the spinal rod. The edges of top section 104 and/or bottom section 106 may contact the spinal rod to prevent the pivoting of the fixation component about the spinal rod beyond a selected degree. Top section 104 preferably contains a curved edge 108, and bottom section 106 preferably contains a curved edge 110. Curved edges 108 and 110 preferably increase the degree that the fixation component can pivot and allow a fixation device (e.g., bone screw 14) to form an angle within a selected range that is perpendicular with or oblique to the spinal rod.
[0073] In an embodiment of the invention, body 80 is laterally offset from the spinal rod. Body 80 may contain a spacer 114 that extends laterally to offset a fixation component from the spinal rod. Offsetting a fixation component from the spinal rod may reduce the degree that the spinal rod must be contoured for proper positioning of bone screws (e.g., pedicle screws) in regions of the spine such as the lower lumbar region. The offset between the fixation component and the spinal rod may be equal to the width of the spacer. The offset is preferably less than about 15 mm, more preferably less than about 10 mm, and more preferably still between about 3 mm and about 9 mm.
[0074] The spacer may contain a tapered cavity for receiving connector 16 as illustrated in FIG. 9. In an embodiment, the spacer contains a first plurality of protrusions or teeth that are adapted to form an engagement with a second plurality of protrusions or teeth 120 disposed on a surface of a fixation device. The teeth of the spacer and the teeth of the fixation device preferably are radially spaced at a fixed spacing 118. The teeth of the spacer and the protrusions of the fixation device preferably form a complementary fit such that adjacent, opposing teeth contact one another over interface length 116 when fastener 18 is tightened. The complementary engagement of the teeth preferably inhibits and/or prevents the fixation device from rotating about spacer 114, thereby fixing the angle formed between the fixation device and the spinal rod.
[0075] An embodiment including a reversible fixation device is illustrated in FIG. 10. The body 80 of the hook preferably includes a first U-shaped yoke 137 disposed on a first side 134 of the body and a second U-shaped yoke 138 disposed on a second side 136 of the body. A cavity 132 preferably extends through the body from the first side 134 to the second side 136. The cavity preferably contains a pair of tapered inner surfaces 133 and 135 that taper in opposite directions such that the cavity narrows in a direction from the first side 134 to the middle of the cavity and narrows in a direction from the second side 136 to the middle of the cavity. The tapered inner surfaces preferably each terminate in an engaging portion 130 disposed in the middle of the cavity. Connector 16 may be positioned within the cavity so that the receiving end extends from either first side 134 as shown in FIG. 10B or from second side 136 as shown in FIG. 10C. Thus, the reversible hook may be mounted so that either first side 134 or second side 136 is proximate the spinal rod, with the hook directed toward either the caudal or cranial direction in each case. The fixation component may contain a slot 109 through which the fastening end of the connector may be inserted during assembly of the construct. The engaging portion 130 preferably engages the outer surface of the receiving end to limit the extent to which the receiving end may be inserted into cavity 132. Fastener 18 preferably engages body 80 proximate the engaging portion.
[0076] An alternate embodiment including a spacer 114 is illustrated in FIG. 11. The spacer preferably surrounds a portion of connector 16 and contains a tapered surface 140 corresponding to the outside surface of the arms of the receiving end. As fastener 18 is tightened, the connector is preferably drawn within the spacer whereby surface 140 engages and exerts a clamping force against the outer surface of the receiving end. A tensile force created by the tightening of fastener 18 preferably maintains the spacer in a fixed position between body 80 and the spinal rod. The tapered surface 140 may terminate in an engaging surface 142 that engages the receiving end, thereby limiting the extent to which the receiving end may be drawn within the spacer. The receiving end preferably forms a “pinch clamp” about the spinal rod, wherein the tips 72 and 74 of the arms terminate slightly beyond a vertical axis 144, which extends through the center of the spinal rod. The fastener may be fully tightened to create a selected offset length 145 that is preferably between about 2 mm and about 10 mm.
[0077] To surgically install spinal fixation system 10, the threaded end of connector 16 is preferably inserted through the tapered cavity of a spinal fixation component and fastener 18 is loosely threaded onto the threaded end. The spinal fixation component is then attached to the spine via a hook or screw in a selected location. A plurality of spinal fixation components may be attached to the spine in like manner. Spinal rod 11 may be contoured to match the desired curvature of the spine and placed into the surgical opening. The spinal rod is preferably snapped within the borehole of the connector of each spinal fixation component. The spine is preferably manipulated such that each of the vertebra is at a selected angle and height relative to neighboring vertebrae and then each fastener 18 is fully tightened to fixably secure the spinal rod into the borehole of each connector and to secure each of the spinal fixation devices at a selected angle relative to the spinal rod. It is generally preferred that the only assembly of system components that occurs within the surgical wound is (a) the snapping of the spinal rod within one or more connectors and (b) the final tightening of one or more fasteners that have already been engaged with the fastening end. Each of the fasteners is preferably tightened with a torque of at least 150 lb-in. One or more transverse connectors may be added across neighboring spinal rods for support to increase the strength of the overall construct and maintain the spinal rods at a fixed distance from one another.
[0078] In an alternate embodiment, each connector and spinal fixation component can be preassembled on the spinal rod prior to the implantation of the rod into the surgical wound. A connector may first be snapped onto the spinal rod. A fixation component may be added onto the connector such that the fastening end of the connector extends through the tapered cavity and the arms of the receiving end contact the inner surface of the tapered cavity. The fastener is preferably positioned on the fastening end and partially tightened to maintain the connector and fixation component engaged with the spinal rod. The fastener is preferably loosely secured on the fastening end to allow the connector and fixation component to slide along the length of the rod when a selected force is applied to the connector. The spinal rod may be contoured as necessary, and the pre-assembled system may be inserted within the surgical wound. The location of the spinal fixation components may be adjusted along the length of the rod as necessary, and the construct may be connected to the spine via fixation devices. Once a fixation component is placed at a selected location, its corresponding fastener may be fully tightened to fix its location. Fixation components may be added to or deleted from the construct as necessary without altering the position of the spinal rod or other fixation components.
[0079] In an alternate embodiment, the system may be partially pre-assembled such that a number of connectors are initially snapped onto the spinal rod. Fixation components may be inserted within the surgical wound and connected to the spine at selected locations via fixation devices. The rod may be selectively contoured and inserted within the surgical wound and aligned proximate the spine. A connector is preferably slid along the rod to a selected location proximate a fixation component on the spine, and the fastening end of the connector is inserted through the tapered cavity of the fixation component. A fastener may be placed on the fastening end to clamp the connector onto the spinal rod and to secure the fixation component therebetween. Additional connectors and fixation components may be secured to the spinal rod in like manner.
[0080] After the rod is implanted into the surgical wound, it may be necessary to add or delete a fixation component. Conventional systems tend to require that the spinal rod be removed from the surgical wound to allow a fixation component to be threaded onto or removed from the rod. In addition, fixation components of conventional systems may have to be removed from the construct to slide the added fixation component to a selected position. Connector 16 is preferably snapped onto the spinal rod at a selected location. Thus, a connector and any fixation device (e.g., screw, hook, transverse connector) may be added to the spinal rod without removing fixation components from the spinal rod or removing the spinal rod from the surgical wound. In the same manner, a connector and fixation device may be removed from the spinal rod without altering the position of the spinal rod or adjacent connectors. The fastener 18 may be loosened and a tool may be used to unclamp the receiving end of the connector from the spinal rod, thereby eliminating the need to slide the component off the end of the spinal rod as in some conventional systems.
Further Improvements
[0081] The following embodiments may be used in combination with any of the features of the above-described embodiments.
[0082] An embodiment of a spinal fixation system that is assembled with a threadless wedge is depicted in FIG. 12 and FIG. 13. FIG. 12 depicts the spinal fixation system prior to assembly. The spinal fixation system preferably includes connector 216 for attaching spinal rod 12 to fixation component body 80. Connector 216 preferably includes a receiving end that includes a pair of deflectable arms forming a substantially U-shaped borehole for receiving the spinal rod as in the above described embodiments. The outer surface of the receiving end may be tapered to complement the tapered inner surface of the cavity disposed within the fixation component. The outer surface of the receiving end and the tapered inner surface may be substantially flat. It is to be understood that the outer surface of the connector may be untapered while the inner surface of the cavity is tapered, or alternatively, the outer surface of the connector may be tapered while the inner surface of the cavity is untapered. The end of the connector opposite the receiving end may be capped as shown in FIG. 12.
[0083] An instrument 200 is preferably used to move the connector through the cavity to cause the arms of the connector to damp against the spinal rod to secure it within the borehole. The instrument is preferably a pair of assembly pliers that includes a first member 202 and a second member 204. Members 202 and 204 are preferably substantially elongated and capable of moving relative to one another to apply a compressive force onto components of the spinal fixation system to assemble the components. The members are preferably connected together via hinge 206. The hinge may include a pivotal connector (e.g., bolt) about which the members can pivot relative to one another.
[0084] One of the members preferably includes an indention 210 for engaging the spinal rod. The indention preferably has a curvate shape that conforms to the shape of the spinal rod. The other member preferably includes a bore 208 that is sized to receive the end of the connector. Bore 208 preferably has a width that is greater than that of the end of the connector such that the end is capable of passing into or through the bore. Member 204 preferably includes contacting sections 214 that surround bore 208 for engaging the fixation component. FIG. 13 depicts the spinal fixation system after assembly. Member 202 preferably engages the spinal rod at indention 210, while member 204 engages the fixation component with contacting sections 214. The handles of instrument 200 are preferably squeezed together to decrease the distance between members 202 and 204, thereby forcing the connector to move within the cavity of the fixation component. The end of the connector preferably moves through the cavity and into bore 208 whereby second member 204 does not inhibit the movement of the connector through the cavity. A locking taper engagement between the connector and the spinal rod is preferably formed, and then instrument 200 may be removed from the assembly. In an alternate embodiment, member 202 engages the tips of the arms of the connector rather than the spinal rod.
[0085] In an embodiment depicted in FIG. 14, the fixation component includes a bore 222 through its top surface that communicates with the fixation component cavity. A locking element 220 is preferably inserted into bore 222 to inhibit movement of the connector within the fixation component cavity after the connector has been secured therein. Locking element 220 is preferably a set screw. Bore 222 is preferably threaded for engaging threads on the set screw. The locking element may engage the connector proximate indention 218 disposed on the outer surface of the connector.
[0086] In an embodiment depicted in FIG. 15, fixation component 230 preferably includes a tapered cavity for receiving connector 216 as in the above described embodiments. The fixation system preferably includes a sleeve 234 that is adapted to fit about the body of the fixation component. The sleeve is preferably substantially cylindrical and may substantially surround the fixation component body. The sleeve preferably includes a substantially U-shaped opening 236 sized to permit spinal rod 12 to pass therethrough. The U-shaped opening is preferably substantially offset from the center of the sleeve as shown in FIG. 15. Opening 236 may include an angled interior locking surface 237 for engaging the spinal rod. Fixation component 230 preferably includes a fastening end 232 on its top. Fastening end 232 preferably includes threading. A fastener 238 is preferably securable to the fastening end. Fastener 238 is preferably a nut that includes threading that complements the threading on the fastening end.
[0087] FIG. 16 depicts a side view of the spinal fixation system after assembly, and FIG. 17 depicts a cross sectional view of the assembled spinal fixation system. To assemble the system, the spinal rod is preferably snapped into the borehole of connector 216. A circumferential portion of the spinal rod preferably extends from the opening in the connector. The connector having the spinal rod disposed therein is then preferably positioned within the cavity of the fixation component. Sleeve 234 is preferably slid over fastening end 232 and around the body of the fixation component until locking surface 237 contacts the spinal rod. Fastener 238 may be threaded onto the fastening end such that the bottom surface of the fastener contacts the top of sleeve 234. Rotation of the fastener preferably downwardly translates the fastener along the fastening end and forces sleeve 234 down along the body of the fixation component. The angle 239 of locking surface 237 from a vertical axis allows the downward motion of the sleeve to impart a force on the spinal rod in a direction axially through the tapered cavity. Angle 239 preferably ranges from about 10 to 30 degrees. The distance that connector 216 moves within the tapered cavity is preferably a function of the degree to which fastener 238 is tightened. It is preferred that a locking taper engagement is formed between the connector and the fixation body cavity after fastener 238 is tightened.
[0088] In an embodiment, depicted in FIG. 18, fixation component 300 preferably includes a body 302 and a fixation device 304. The body 302 preferably includes a cavity 318 (shown in FIG. 19) adapted to receive a connector 216. The body 302 may include a substantially U-shaped indentation 306 adapted to permit a portion of spinal rod 12 to rest within the indentation. The indentation 306 preferably runs along the bottom 312 of the body 302 in a direction substantially perpendicular to the longitudinal axis of the fixation device 304. The body 302 may include a bore (not shown) that communicates with the cavity 318. A locking element is preferably inserted into the bore to inhibit movement of the connector 216 within the body cavity 318 after the connector has been secured therein.
[0089] The body 302 is preferably adapted to hold a fixation device 304. The fixation device 304 preferably includes a head 310. The head 310 may be semi-spherical in shape. An opening (not shown) may extend through the central portion of the head 310, at a position equidistant from any position along the semi-spherical portion of the outside surface of the head. The fixation device may a bone screw (as shown), hook, traverse connector, or similar device. The body 302 may include a cavity 318 (shown in FIG. 19) adapted to contain a portion of the head 310. A substantially cylindrical pin 308 is preferably positionable within the head 310 and the body 302 such that the fixation device 304 may be rotated about the pin 308 along the longitudinal axis of the body. The pin 308 may inhibit movement of the fixation device 304 in a direction perpendicular to the longitudinal axis of the body 302. The pin 308 may be a rivet or a screw. The pin 308 may be substantially hollow.
[0090] FIG. 19 depicts a top view of the fixation component 300. The cavity 318 may be substantially U-shaped and include a front section 306 and a rear section 308. The front section 306 is preferably adapted to receive the fixation device 304. The front section 306 preferably includes at least two substantially flat arms 320 which extend out from the rear section 308. The arms 320 are preferably oriented on opposing sides of the body 302. The distance 322 between the two arms 320 may be substantially greater than the width of the head 310 of the fixation device 304. It is generally preferred that the distance 322 between the two arms 320 and the width of the head 310 be equal.
[0091] In another embodiment, the head 310 of the fixation device 304 may have at least two substantially flat edges 324. The distance 322 between the two arms 320 is preferably substantially the same as the width of the head 310 between the edges 324. The edges 324 are preferably oriented on opposing sides of the head 310. The fixation device 304 may be , mounted within the cavity 318 such that the edges 324 are contained by the arms 320 of the body 302. The arms 320 may interact with the edges 324 such that movement in a direction perpendicular to the longitudinal axis of the body 302 is inhibited.
[0092] The rear section 308 of the cavity 318 is substantially rounded and adapted to receive a connector 216. FIG. 20 depicts a cross sectional view of the fixation component 300, secured to a spinal rod 12, with a connector 216 oriented within the rear section of the cavity. Connector 216 preferably includes a receiving end that includes a pair of deflectable arms forming a substantially U-shaped borehole for receiving the spinal rod, as described in previous embodiments. The width of the body 302 between the rear side 328 and the interior surface 326 of the cavity 318 is preferably variable. The distance between the rear side 328 and the interior surface 326 of the body 302 preferably becomes narrower in a direction from the top 314 toward the bottom 312. The interior surface 326 of the body 302 may be substantially flat.
[0093] The head 310 of the fixation device 304 is preferably located within the body 302 in a position such a portion of the connector 216 may be inserted between the head and the interior surface 326. Movement of the connector 216 through the bottom 312 of the body 302, in a direction toward the top 314, may allow the outer edges 330 of the connector to engage the interior surface 326 of the body and the head 310 of the fixation device 304. As the connector 216 is moved further toward the top 314 of the body 302, a compressive force may be exerted by the interior surface 326 and the head 341 upon the connector. The magnitude of the compressive force may be varied as the position of the connector 216 is varied within the cavity. The compressive force preferably secures spinal rod 12 within the U-shaped borehole of the connector 216. The compressive force may inhibit rotation of the fixation device 304. Instrument 200 (not shown) may be used to position the connector 216 within the body 302 in a position which preferably secures the spinal rod to the connector. The connector 216 may be positioned within the body 302 such that the spinal rod 12 is secured within the connector, and the rotation of the fixation device 304 is inhibited.
[0094] FIG. 18 depicts a view of an assembled spinal fixation assembly. To assemble the system the spinal rod 12 is snapped into the borehole of connector 216. A circumferential portion of the spinal rod 12 preferably extends from the borehole in the connector 216. The connector 216 having the spinal rod 12 disposed therein is then preferably positioned within the body 302. The fixation device 304 may be rotated about the pin 308 until the desired angle between the body 302 and the fixation device is achieved. The angle may be varied in a direction toward the top 314 through an arc of at least, 90 degrees or toward the bottom 312 through an arc of at least 90 degrees. The connector 216 may then be moved further within the body 302. As the connector 216 is moved, the head 310 and the interior surface 326 of the body 302 may impart a force upon the connector (as shown in FIG. 20) causing the arms of the borehole to compress. In this manner the connector 216 may be secured onto the spinal rod 12. The force may also inhibit further rotation of the fixation device 304. The magnitude of the force is preferably a function of the distance that the connector 216 is placed within the body 302. Instrument 200 may be used to position the connector 216 within the body 302.
[0095] An embodiment of a connector 350 is depicted in FIG. 21. The connector 350 is adapted to secure fixation components to a spinal rod. The substantially conical connector 350 includes a receiving section 352 and an upper section 354. The receiving section 352 preferably includes a substantially circular opening 356. The opening 356 is preferably adapted to receive a spinal rod (not shown) such that the receiving section 352 of the connector 350 substantially surrounds the circumferential portion of the spinal rod. The upper section 354 preferably includes a slot 358 extending longitudinally through the center of the upper section. The slot 358 may extend from the top of the connector to the opening 356, the slot communicating with the opening.
[0096] A spinal rod is preferably axially positioned within the opening 356 by passing the spinal rod through opening. Slot 358 preferably enables the circumference of opening 356 to be altered. Insertion of the spinal rod into opening 356 results in a slight widening of at least a portion of the slot 358. In this manner, the circumference of opening 356 may be increased by an amount sufficient to allow the insertion of the spinal rod through opening 356. If the diameter of the spinal rod is slightly greater than that of the opening 356, the slot 358 may remain slightly widened after the spinal rod is inserted into the opening. It is generally preferred that the diameter of the spinal rod and the diameter of the opening 356 be equal.
[0097] FIG. 22 depicts a cross sectional view of an assembled spinal fixation assembly including a connector 350 and a fixation component 300. Movement of the connector 350 through the bottom 312 of the body 302, in a direction toward the top 314, may allow the outer edges 360 of the connector to engage the interior surface 326 of the body and the head 310 of the fixation device 304. As the connector 350 is moved further toward the top 314 of the body 302, a compressive force may be exerted by the interior surface 326 and the head 310 upon the connector. The magnitude of the compressive force may be varied as the position of the connector 350 is varied within the cavity. The compressive force preferably forces slot 358 to narrow, thereby securing spinal rod 12 within the opening 356 of the connector 350. The compressive force may inhibit rotation of the fixation device 304. Instrument 200 (not shown) may be used to position the connector 350 within the body 302 in a position which preferably secures the spinal rod 12 within the connector. The connector 350 may be positioned within the body 302 such that the spinal rod 12 is secured within the connector, and the rotation of the fixation device 304 is inhibited.
[0098] To assemble the system depicted in FIG. 22 the spinal rod 12 is inserted into the opening 356 of connector 350. A circumferential portion of the spinal rod 12 preferably is completely surrounded by the connector 350. The connector 350 having the spinal rod 12 disposed therein is then preferably positioned within the body 302. The fixation device 304 may be rotated about the pin 308 until the desired angle between the body 302 and the fixation device is achieved. The connector 350 may then be moved further within the body 302. As the connector 350 is moved, the head 310 and the interior surface 326 of the body 302 may impart a force upon the connector causing the slot 358 of the connector to narrow. In this manner the connector 350 may be secured onto the spinal rod 12. The force may also inhibit further rotation of the fixation device 304. The magnitude of the force is preferably a function of the distance that the connector 350 is placed within the body 302. Instrument 200 may be used to position the connector 350 within the body 302.
[0099] In an embodiment depicted in FIG. 23, fixation component 230 may be adapted to receive connector 350. Connector 350 preferably includes an opening 356 for receiving the spinal rod 12 and a slot 358 (shown in FIG. 24) as in the above described embodiments. The fixation component 230 preferably can be pivoted in either direction 362 or direction 364 such that an oblique angle between 90° and about 60° is formed between the fixation component and the longitudinal axis of the spinal rod 12 as in the above described embodiments. The fixation component 230 preferably comprises a bone screw (as shown), hook, traverse connector, or similar device.
[0100] To assemble the system, depicted in a cross section view in FIG. 24, the spinal rod 12 is preferably inserted into the opening 356 of connector 350. The connector 350 having the spinal rod 12 disposed therein is then preferably positioned within the cavity of the fixation component 230. The fixation component 230 may be rotated until the desired angle between the fixation component and the longitudinal axis of the spinal rod is achieved. The connector 350 may then be moved further within the fixation component 230. As the connector 350 is moved, the interior surfaces 366 of the fixation component may impart a force upon the connector causing the slot 358 of the connector to narrow. In this manner the connector 350 may be secured onto the spinal rod 12. The force may also inhibit further rotation of the fixation component 230. The magnitude of the force is preferably a function of the distance that the connector 350 is placed within the body 302. Instrument 200 (not shown) may be used to position the connector 350 within the body 302.
[0101] Further modifications and alternative embodiments of various aspects of the invention will be apparent to those skilled in the art in view of this description. Accordingly, this description is to be construed as illustrative only and is for the purpose of teaching those skilled in the art the general manner of carrying out the invention. It is to be understood that the forms of the invention shown and described herein are to be taken as the presently preferred embodiments. Elements and materials may be substituted for those illustrated and described herein, parts and processes may be reversed, and certain features of the invention may be utilized independently, all as would be apparent to one skilled in the art after having the benefit of this description of the invention. Changes may be made in the elements described herein without departing from the spirit and scope of the invention as described in the following claims.
Claims
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What is claimed is:
1. An implant system for fixation of the human spine, comprising:
a connector comprising a receiving end terminating in a first arm and a second arm that together form a substantially U-shaped borehole, the first arm comprising a first tip and the second arm comprising a second tip, and wherein an opening is formed between the first tip and the second tip;
a spinal rod axially positionable through the opening into the borehole during use; and
a fixation component comprising a body, the body comprising a tapered cavity having an inner surface, the tapered cavity being adapted to receive the connector such that the inner surface engages the first arm and the second arm, and a fixation device for attaching the spinal rod to a vertebra during use;
and wherein the receiving end is moveable within the tapered cavity to cause deflection of the first and second arms such that the first and second arms exert a compressive force against the spinal rod to maintain the spinal rod within the borehole during use.
2. The implant system of claim 1 wherein the spinal rod comprises a diameter, and wherein the opening has a width defined by the first tip and the second tip, and wherein the width is adjustable by moving the receiving end within the tapered cavity.
3. The implant system of claim 1 wherein the first and second arms are deflectable in a direction toward one another and in a direction away from one another.
4. The implant system of claim 1 wherein the spinal rod is positioned within the borehole and wherein a portion of the spinal rod is exposed from the receiving end of the connector.
5. The implant system of claim 1 wherein the connector further comprises a slot extending adjacent to the receiving end, and wherein the tapered cavity comprises a first end and a second end, the tapered cavity being narrower at a location proximate the second end than at a location proximate the first end, and wherein movement of the receiving end within the tapered cavity causes deflection of the first arm and the second arm such that a portion of the slot narrows and the arms exert a compressive force against the spinal rod to clamp the spinal rod within the borehole.
6. The implant system of claim 1 wherein the spinal rod comprises a cross-section having a circumferential portion, and wherein between about π radians and about 2π radians of the circumferential portion is surrounded by the receiving end.
7. The implant system of claim 1 wherein the fixation device further comprises a bone screw having a shank.
8. The implant system of claim 1 wherein the fixation device further comprises a hook for engaging a bone.
9. The implant system of claim 1 wherein the system further comprises a transverse connector for connecting the spinal rod to a neighboring spinal rod at a fixed distance.
10. The implant system of claim 1 wherein the body comprises a substantially U-shaped yoke having an axial length, the yoke being formed between a top section and a bottom section, the top section comprising a first edge, the bottom section comprising a second edge, the first and second edges defining a width of the yoke, and wherein the first and second edges are curved such that the width of the yoke varies across the axial length of the yoke.
11. The implant system of claim 1 wherein the fixation component further comprises a spacer adapted to fit between the connector and the fixation device to laterally offset the fixation device from the spinal rod.
12. The implant system of claim 1 wherein the fixation component further comprises a spacer, the spacer being adapted to fit between the connector and the fixation component, the fixation device comprising protrusions, the spacer being adapted to offset the fixation device from the spinal rod and comprising teeth adapted to form a complementary engagement with the protrusions to inhibit rotation of the fixation device about the spacer.
13. The implant system of claim 1 wherein the body further comprises a top section and a bottom section, the tapered cavity being formed in between the top section and the bottom section, the top section and the bottom section each comprising edges that are curved in a direction away from the spinal rod.
14. The implant system of claim 1 wherein the fixation component further comprises a bore, and further comprising a locking element adapted to extend through the bore and contact the connector to inhibit movement of the connector within the tapered cavity.
15. The implant system of claim 1 wherein the compressive force exerted against the spinal rod is selectively variable and is a function of a depth of the receiving end within the tapered cavity.
16. The implant system of claim 1 wherein the system further comprises a transverse connector connecting the spinal rod to a neighboring spinal rod, the transverse connector comprising a reduced section and a beveled section, the reduced section having a width less than a width of the body, the beveled section connecting the reduced section to the body.
17. The implant system of claim 1 wherein the receiving end comprises a tapered outer surface that narrows in a direction away from the receiving end.
18. The implant system of claim 1 wherein the spinal rod is positioned within the borehole, and wherein a portion of the spinal rod is exposed from the borehole, and wherein the exposed portion extends from the borehole through the opening.
19. The implant system of claim 1 wherein the body comprises a substantially U-shaped yoke having an axial length defined between a pair of outer edges, the yoke being formed between a top section and a bottom section, the top section comprising a first edge, the bottom section comprising a second edge, the first and second edges defining a width of the yoke, and wherein the first and second edges are curved such that the width of the yoke varies across the axial length of the yoke, and wherein the width of the yoke is greater at one of the outer edges of the yoke than at a location between the outer edges of the yoke.
20. The implant system of claim 1 wherein the first and second arms are deflectable to form a locking taper engagement with the spinal rod.
21. The implant system of claim 1, further comprising a slot in the connector, the slot enabling the first arm and the second arm to be deflected relative to one another.
22. The implant system of claim 1 further comprising a slot in the connector, the slot communicating with the receiving end and enabling the spinal rod to be snappingly engaged within the borehole.
23. An implant system for fixation of the human spine, comprising:
a connector comprising a receiving end forming a substantially U-shaped borehole having an open end;
a spinal rod axially positionable through the open end into the borehole during use, the spinal rod being fixable within the borehole by a clamping force exerted by the connector; and
a fixation component comprising a body, the body comprising a cavity having an inner surface, and wherein the connector is adapted to be at least partially disposed within the cavity such that the inner surface of the cavity engages and exerts a compressive force onto an outer surface of the receiving end to maintain the spinal rod within the borehole, and a threaded bore and a screw adapted to extend through the bore and contact the connector to inhibit movement of the connector within the tapered cavity during use.
24. The implant system of claim 23 wherein the receiving end comprises a first arm having a first tip and a second arm having a second tip, the first arm and the second arm together forming the substantially U-shaped borehole, and wherein an opening is defined between the first tip and the second tip.
25. The implant system of claim 23 wherein the receiving end comprises a first arm having a first tip and a second arm having a second tip, the first arm and the second arm together forming the substantially U-shaped borehole, and wherein an opening is defined between the first tip and the second tip, and wherein the opening has a width that is adjustable by moving the connector within the cavity.
26. The implant system of claim 23 wherein the cavity of the body is a tapered cavity having a first end and a second end, and wherein the tapered cavity narrows in a direction from the first end to the second end.
27. The implant system of claim 23 wherein the cavity of the body is a tapered cavity having a first end and a second end, and wherein the tapered cavity narrows in a direction from the first end to the second end, and wherein the tapered cavity is adapted to substantially surround a portion of the receiving end and impart a compressive force against the receiving end to fixably secure the spinal rod within the borehole.
28. The implant system of claim 23 wherein the receiving end further comprises a first arm having a first tip and a second arm having a second tip, the first arm and the second arm together forming the substantially U-shaped borehole, and further comprising a slot in the connector between the receiving end and the fastening end, the slot enabling the first arm and the second arm to be deflected relative to one another, the deflection of the arms causing a change in a distance between the first tip and the second tip.
29. The implant system of claim 23 wherein the fixation component further comprises a bore, and further comprising a locking element adapted to extend through the bore and contact the connector to inhibit movement of the connector within the tapered cavity.
30. The implant system of claim 23 wherein the cavity is a tapered cavity, and wherein the outer surface of the receiving end has a taper that complements that of the tapered cavity, and wherein the receiving end is adapted to be moved within the tapered cavity such that the inner surface of the tapered cavity exerts a compressive force against the outer surface of the receiving end to clamp the spinal rod within the borehole, the compressive force having a magnitude that is a function of a distance that the receiving end is moved into the tapered cavity.
31. The implant system of claim 23 wherein the fixation component further comprises a fixation device for attaching the spinal rod to a vertebra.
32. The implant system of claim 23 wherein the spinal rod comprises a circumferential portion, and wherein greater than about π radians and less than about 2π radians of the circumferential portion is engaged by the receiving end.
33. The implant system of claim 23 wherein the body comprises a substantially U-shaped yoke having an axial length, the yoke being formed between a top section and a bottom section, the top section comprising a first edge, the bottom section comprising a second edge, the first and second edges defining a width of the yoke, and wherein the first and second edges are curved such that the width of the yoke varies across the axial length of the yoke.
34. The implant system of claim 23 wherein the fixation component further comprises a fixation device and a spacer adapted to fit between the connector and the fixation device, the spacer being adapted to laterally offset the fixation device from the spinal rod.
35. The implant system of claim 23 wherein the fixation component further comprises a fixation device and a spacer adapted to fit between the connector and the fixation device, the fixation device comprising protrusions, the spacer offsetting the fixation device from the spinal rod and comprising teeth adapted to form a complementary engagement with the protrusions to inhibit rotation of the fixation device about the spacer.
36. The implant system of claim 23 wherein the body further comprises a top section and a bottom section, the cavity being formed in between the top section and the bottom section, the top section and the bottom section each comprising edges that are curved, and wherein the fixation component is adapted to pivot about the spinal rod in a substantially vertical plane, and wherein the curved edges are adapted to contact the spinal rod during the pivoting of the fixation component, thereby defining a range of pivotal motion of the fixation component.
37. The implant system of claim 23 wherein the system further comprises a transverse connector for connecting the spinal rod to a neighboring spinal rod, the transverse connector comprising a reduced section and a beveled section, the reduced section having a width less than a width of the body, the beveled section being located between the body and the reduced section.
38. The implant system of claim 23 wherein the system further comprises a transverse connector for connecting the spinal rod to a neighboring spinal rod, the transverse connector comprising a reduced section and a beveled section, the reduced section having a width less than a width of the body, the beveled section being located between the body and the reduced section, and wherein the reduced section comprises a bend to shorten a lateral distance between the spinal rod and the neighboring spinal rod.
39. The implant system of claim 23 wherein the spinal rod comprises a diameter, and wherein the open end has a width defined by the first tip and the second tip, and wherein the width is adjustable by moving the connector within the cavity.
40. An implant system for fixation of the human spine, comprising:
a connector comprising a receiving end terminating in a first arm and a second arm that together form a substantially U-shaped borehole, the first arm comprising a first tip and the second arm comprising a second tip, and wherein an opening is formed between the first tip and the second tip;
a spinal rod axially positionable through the opening into the borehole during use; and
a fixation component comprising a body and a fastening end, the body comprising a tapered cavity having an inner surface, the tapered cavity being adapted to receive the connector such that the inner surface engages the first arm and the second arm during use;
a sleeve comprising a substantially U-shaped opening, the sleeve being adapted to fit substantially about the body of the fixation component during use; and
a fastener positionable on the fastening end, the fastener being adapted to move the sleeve to cause the receiving end to move within the tapered cavity, thereby deflecting the first and second arms such that the first and second arms exert a compressive force against the spinal rod to maintain the spinal rod within the borehole during use.
41. The implant system of claim 40 wherein the fastener is a threaded nut.
42. The implant system of claim 40 wherein the fastening end comprises a threaded surface.
43. The implant system of claim 40 wherein the sleeve is substantially cylindrical and adapted to substantially surround the body of the fixation component during use.
44. The implant system of claim 40 wherein the U-shaped opening is substantially offset from a center of the sleeve.
45. The implant system of claim 40 wherein the sleeve comprises an angled interior locking surface adapted to impart a force onto the spinal rod to move the connector within the tapered cavity during use.
46. The implant system of claim 40 wherein the sleeve comprises an interior surface that is adapted to impart a force onto the spinal rod when the sleeve is downwardly translated along the body, the force causing the connector to move into the tapered cavity during use.
47. The implant system of claim 40 wherein the spinal rod comprises a diameter, and wherein the opening has a width defined by the first tip and the second tip, and wherein the width is adjustable by moving the receiving end within the tapered cavity.
48. The implant system of claim 40 wherein the first and second arms are deflectable in a direction toward one another and in a direction away from one another.
49. The implant system of claim 40 wherein the connector further comprises a slot extending adjacent to the receiving end, and wherein the tapered cavity comprises a first end and a second end, the tapered cavity being narrower at a location proximate the second end than at a location proximate the first end, and wherein movement of the receiving end within the tapered cavity causes deflection of the first arm and the second arm such that a portion of the slot narrows and the arms exert a compressive force against the spinal rod to clamp the spinal rod within the borehole.
50. The implant system of claim 40 wherein the spinal rod comprises a cross-section having a circumferential portion, and wherein between about π radians and about 2π radians of the circumferential portion is surrounded by the receiving end.
51. The implant system of claim 40 wherein the fixation component further comprises a bone screw having a shank.
52. The implant system of claim 40 wherein the fixation component further comprises a hook for engaging a bone.
53. The implant system of claim 40 wherein the fixation component further comprises a transverse connector for connecting the spinal rod to a neighboring spinal rod at a fixed distance.
54. The implant system of claim 40 wherein the body comprises a substantially U-shaped yoke having an axial length, the yoke being formed between a top section and a bottom section, the top section comprising a first edge, the bottom section comprising a second edge, the first and second edges defining a width of the yoke, and wherein the first and second edges are curved such that the width of the yoke varies across the axial length of the yoke.
55. The implant system of claim 40 wherein the body further comprises a top section and a bottom section, the tapered cavity being formed in between the top section and the bottom section, the top section and the bottom section each comprising edges that are curved in a direction away from the spinal rod.
56. The implant system of claim 40 wherein the compressive force exerted against the spinal rod is selectively variable and is a function of a depth of the receiving end within the tapered cavity.
57. The implant system of claim 40 wherein the fixation component further comprises a transverse connector connecting the spinal rod to a neighboring spinal rod, the transverse connector comprising a reduced section and a beveled section, the reduced section having a width less than a width of the body, the beveled section connecting the reduced section to the body.
58. The implant system of claim 40 wherein the fixation component further comprises a transverse connector connecting the spinal rod to a neighboring spinal rod, the transverse connector comprising a reduced section and a beveled section, the reduced section having a width less than a width of the body, the beveled section extending between the body and the reduced section, and wherein the reduced section comprises a bend to shorten a lateral distance between the spinal rod and the neighboring spinal rod.
59. The implant system of claim 40 wherein the receiving end comprises a tapered outer surface that narrows in a direction away from the receiving end.
60. The implant system of claim 40 wherein the body comprises a substantially U-shaped yoke having an axial length defined between a pair of outer edges, the yoke being formed between a top section and a bottom section, the top section comprising a first edge, the bottom section comprising a second edge, the first and second edges defining a width of the yoke, and wherein the first and second edges are curved such that the width of the yoke varies across the axial length of the yoke, and wherein the width of the yoke is greater at one of the outer edges of the yoke than at a location between the outer edges of the yoke.
61. The implant system of claim 40 wherein the first and second arms are deflectable to form a locking taper engagement with the spinal rod.
62. The implant system of claim 40, further comprising a slot in the connector, the slot enabling the first arm and the second arm to be deflected relative to one another.
63. The implant system of claim 40 further comprising a slot in the connector, the slot communicating with the receiving end and enabling the spinal rod to be snappingly engaged within the borehole.
64. An implant system for fixation of the human spine, comprising:
a connector comprising a receiving end forming a substantially U-shaped borehole;
a spinal rod axially positionable within the borehole during use; and
a fixation component comprising a body and a fastening end, the body comprising a cavity having an inner surface, the cavity being adapted to receive the connector such that the inner surface engages an outer surface of the receiving end during use;
a sleeve comprising a substantially U-shaped opening, the sleeve being adapted to fit substantially about the body of the fixation component during use; and
a fastener positionable on the fastening end, the fastener being adapted to move the sleeve to cause the receiving end to move within the cavity, thereby deflecting the receiving end to exert a compressive force against the spinal rod to maintain the spinal rod within the borehole during use.
65. The implant system of claim 64 wherein the fixation component further comprises a fixation device for attaching the spinal rod to a vertebra.
66. A method of surgically implanting a spinal fixation system comprising:
connecting a fixation component to a portion of a spine, the fixation component comprising a body, the body comprising a cavity having an inner surface;
positioning a connector within the cavity, the connector comprising a receiving end forming a substantially U-shaped borehole having an open end, and wherein the connector is positioned within the cavity such that the inner surface of the cavity engages an outer surface of the receiving end;
snapping a spinal rod through the open end of the borehole; and
moving the connector within the cavity to translate a sleeve along the body of the fixation component and cause the inner surface of the cavity to exert a compressive force onto the outer surface of the receiving end such that the receiving end is clamped onto the spinal rod to maintain the spinal rod within the borehole.
67. The method of claim 66 wherein the cavity is a tapered cavity having a first end and a second end, the tapered cavity narrowing in a direction from the first end to the second end, and wherein moving the connector within the tapered cavity in a direction from the first end to the second end causes the tapered cavity to exert a compressive force against the receiving end to deflect the receiving end and cause the receiving end to clamp the spinal rod within the borehole.
68. The method of claim 66, further comprising clamping a connector onto the spinal rod after the spinal rod has been attached to the spine portion, the connector being clamped onto the spinal rod without detaching the spinal rod from the spine portion.
69. The method of claim 66, further comprising clamping a connector onto the spinal rod after the spinal rod has been attached to the spine portion, the connector being clamped onto the spinal rod without removing other connectors from the spinal rod.
70. The method of claim 66, further comprising clamping a connector onto the spinal rod after the spinal rod has been attached to the spine portion, the connector being clamped onto the spinal rod without detaching the spinal rod from the spine portion and without altering a position of any other connectors engaged to the spinal rod.
71. The method of claim 66 wherein a portion of the spinal rod extends from the open end of the borehole after the receiving end is clamped onto the spinal rod.
72. The method of claim 66 wherein the spinal rod comprises a circumferential portion, and wherein the receiving end surrounds greater than about π radians of the circumferential portion and less than about 2π radians of the circumferential portion after the receiving end is clamped onto the spinal rod.
73. The method of claim 66, further comprising applying a distraction force to the connector to change the location of the connector on the spinal rod after the connector has been moved within the cavity to tighten the receiving end about the spinal rod.
74. The method of claim 66 wherein the fixation component is attached to the spine portion with a bone screw, and further comprising pivoting the bone screw about the spinal rod to form an oblique angle between the bone screw and a longitudinal axis of the spinal rod.
75. The method of claim 66, further comprising removing a connector from the spinal rod after the spinal rod has been attached to the spine portion, the connector being removed without detaching the spinal rod from the spine portion and without altering a position of any other connectors engaged to the spinal rod.
76. The method of claim 66 the connector is moved within the cavity and the fixation component is connected to the spine portion before the spinal rod is snapped into the borehole.
77. The method of claim 66, further comprising positioning a locking element through a bore of the fixation component, the locking element engaging the connector to maintain it fixed within the cavity.
78. The method of claim 66 wherein moving the connector within the cavity comprises compressing the fixation component and the connector together with a tool.
79. The method of claim 66 wherein the fixation component comprises a fastening end, and wherein moving the connector within the cavity comprises tightening a fastener located on the fastening end.
80. The method of claim 66 wherein the fixation component comprises a threaded fastening end, and wherein moving the connector within the cavity comprises tightening a nut located on the fastening end.
81. An implant system for fixation of the human spine, comprising:
a connector comprising a lower section and an upper section, the lower section defining an opening, the upper section defining a slot communicating with the opening;
a spinal rod axially positionable through the opening during use such that the opening substantially surrounds a circumferential portion of the spinal rod; and
a fixation component comprising a body, the body comprising a tapered cavity having an inner surface, the tapered cavity being adapted to receive the connector such that the inner surface engages an outer surface of the connector, and a fixation device for attaching the spinal rod to a vertebra during use;
and wherein the connector is moveable within the tapered cavity to cause a width of the slot to vary such that a width of the opening is altered, and wherein the lower section exerts a compressive force against the spinal rod to maintain the spinal rod within the opening during use.
82. The implant system of claim 81 wherein the tapered cavity comprises a first end and a second end, the tapered cavity being narrower at a location proximate the second end than at a location proximate the first end, and wherein movement of the connector within the tapered cavity causes a portion of the slot to narrow such that the lower section exerts a compressive force against the spinal rod to clamp the spinal rod within the opening.
83. The implant system of claim 81 wherein the fixation component further comprises a spacer configured to abut a portion of the connector, wherein the spacer comprises teeth, wherein a fixation device comprises protrusions, and wherein the teeth are configured to engage the protrusions during use to inhibit rotation of the rod positioned within the connector opening relative to the fixation device.
84. The implant system of claim 81 wherein the body further comprises a top section and a bottom section, the tapered cavity being formed in between the top section and the bottom section, the top section and the bottom section each comprising edges that are curved in a direction away from the spinal rod.
85. The implant system of claim 81 wherein the fixation component further comprises a bore, and further comprising a locking element adapted to extend through the bore and contact the connector to inhibit movement of the connector within the tapered cavity.
86. The implant system of claim 81 wherein the compressive force exerted against the spinal rod is selectively variable and is a function of a depth of the connector within the tapered cavity.
87. The implant system of claim 81 wherein the system further comprises a transverse connector connecting the spinal rod to a neighboring spinal rod, the transverse connector comprising a reduced section and a beveled section, the reduced section having a width less than a width of the body, the beveled section extending between the body and the reduced section, and wherein the reduced section comprises a bend to shorten a lateral distance between the spinal rod and the neighboring spinal rod.
88. The implant system of claim 81 wherein the connector comprises a tapered outer surface that narrows in a direction away from the lower section.
89. The implant system of claim 81 wherein the body comprises a substantially U-shaped yoke having an axial length defined between a pair of outer edges, the yoke being formed between a top section and a bottom section, the top section comprising a first edge, the bottom section comprising a second edge, the first and second edges defining a width of the yoke, and wherein the first and second edges are curved such that the width of the yoke varies across the axial length of the yoke, and wherein the width of the yoke is greater at one of the outer edges of the yoke than at a location between the outer edges of the yoke.
90. An implant system for fixation of the human spine, comprising:
a connector comprising a lower section defining an opening;
a spinal rod axially positionable through the opening during use such that the opening substantially surrounds the circumferential portion of the spinal rod, the spinal rod being fixable within the opening by a clamping force exerted by the connector; and
a fixation component comprising a body, the body comprising a cavity having an inner surface, and wherein the connector is adapted to be at least partially disposed within the cavity such that the inner surface of the cavity engages and exerts a compressive force onto an outer surface of the lower section to maintain the spinal rod within the opening, and a fixation device for attaching the spinal rod to a vertebra during use.
91. The implant system of claim 90 wherein the opening has a width, and wherein the width is adjustable by moving the connector within the cavity.
92. The implant system of claim 90 wherein the connector further comprises a slot communicating with the opening, and wherein the opening has a width that is adjustable by varying the width of the slot.
93. The implant system of claim 90 wherein the connector further comprises a slot communicating with the opening, and wherein the width of the slot is adjustable by varying the position of the connector within the cavity, and wherein the opening has a width that is adjustable by varying the width of the slot.
94. The implant system of claim 90 wherein the cavity comprises a first end and a second end, the cavity being narrower at a location proximate the second end than at a location proximate the first end, and wherein the connector further comprises a slot communicating with the opening such that movement of the connector in a direction from the first end to the second end causes a portion of the slot to narrow such that the lower section exerts a compressive force against the spinal rod to clamp the spinal rod within the opening.
95. The implant system of claim 90 wherein the cavity of the body is a tapered cavity having a first end and a second end, and wherein the tapered cavity narrows in a direction from the first end to the second end, and wherein the tapered cavity is adapted to substantially surround a portion of the connector and impart a compressive force against the connector to fixably secure the spinal rod within the opening.
96. The implant system of claim 90 wherein the fixation component further comprises a bore, and further comprising a locking element adapted to extend through the bore and contact the connector to inhibit movement of the connector within the tapered cavity.
97. The implant system of claim 90 wherein the cavity is a tapered cavity, and wherein the outer surface of the connector has a taper that complements that of the tapered cavity, and wherein the connector is adapted to be moved within the tapered cavity such that the inner surface of the tapered cavity exerts a compressive force against the outer surface of the connector to clamp the spinal rod within the opening, the compressive force having a magnitude that is a function of a distance that the connector is moved into the tapered cavity.
98. The implant system of claim 90 wherein the body comprises a substantially U-shaped yoke having an axial length, the yoke being formed between a top section and a bottom section, the top section comprising a first edge, the bottom section comprising a second edge, the first and second edges defining a width of the yoke, and wherein the first and second edges are curved such that the width of the yoke varies across the axial length of the yoke.
99. The implant system of claim 90 wherein the body further comprises a top section and a bottom section, the cavity being formed in between the top section and the bottom section, the top section and the bottom section each comprising edges that are curved, and wherein the fixation component is adapted to pivot about the spinal rod in a substantially vertical plane, and wherein the curved edges are adapted to contact the spinal rod during the pivoting of the fixation component, thereby defining a range of pivotal motion of the fixation component.
100. The implant system of claim 90 wherein the system further comprises a transverse connector for connecting the spinal rod to a neighboring spinal rod, the transverse connector comprising a reduced section and a beveled section, the reduced section having a width less than a width of the body, the beveled section being located between the body and the reduced section, and wherein the reduced section comprises a bend to shorten a lateral distance between the spinal rod and the neighboring spinal rod.
101. An implant system for fixation of the human spine, comprising:
a connector comprising a receiving end forming a substantially U-shaped borehole having an open end;
a spinal rod axially positionable through the open end into the borehole during use, the spinal rod being fixable within the borehole by a clamping force exerted by the connector; and
a fixation component comprising a fixation device and a body, the fixation device comprising a head, the body comprising a cavity, and wherein a portion of the head is positioned within the cavity; and
wherein the connector is adapted to be at least partially disposed within the cavity such that a portion of the cavity and the head engage and exert a compressive force onto an outer surface of the receiving end to maintain the spinal rod within the borehole during use.
102. The implant system of claim 101 wherein the receiving end comprises a first arm having a first tip and a second arm having a second tip, the first arm and the second arm together forming the substantially U-shaped borehole, and wherein an opening is defined between the first tip and the second tip, and wherein the opening has a width that is adjustable by moving the connector within the cavity.
103. The implant system of claim 101 wherein the cavity further comprises a rear section, and wherein the body further comprises a width, a first section, a second section, and a rear side, and wherein the width is defined by the rear side of the body and an interior surface of the rear section, and wherein the width becomes narrower in a direction from the first section toward the second section of the body, and wherein the interior surface and the fixation device are adapted to concurrently engage separate portions of the receiving end and impart a compressive force against the receiving end to fixably secure the spinal rod within the borehole.
104. The implant system of claim 101 wherein the receiving end further comprises a first arm having a first tip and a second arm having a second tip, the first arm and the second arm together forming the substantially U-shaped borehole, and further comprising a slot in the connector between the receiving end and the fastening end, the slot enabling the first arm and the second arm to be deflected relative to one another, the deflection of the arms causing a change in a distance between the first tip and the second tip.
105. The implant system of claim 101 wherein the fixation component further comprises a bore, and further comprising a locking element adapted to extend through the bore and contact the connector to inhibit movement of the connector within the cavity.
106. The implant system of claim 101 wherein the cavity comprises a rear section, the rear section comprising a tapered interior surface, and wherein the outer surface of the receiving end has a taper that complements that of the tapered interior surface, and wherein the receiving end is adapted to be moved within the cavity such that the tapered interior surface of the cavity and the fixation member together exert a compressive force against the outer surface of the receiving end to clamp the spinal rod within the borehole, the compressive force having a magnitude that is a function of a distance that the receiving end is moved into the cavity.
107. The implant system of claim 101 wherein the fixation device is adapted to attach the spinal rod to a vertebra.
108. The implant system of claim 101 wherein the spinal rod comprises a circumferential portion, and wherein greater than about π radians and less than about 2π radians of the circumferential portion is engaged by the receiving end.
109. The implant system of claim 101 wherein the fixation device is a transverse connector for connecting the spinal rod to a neighboring spinal rod, the transverse connector comprising a reduced section and a beveled section, the reduced section having a width less than a width of the body, the beveled section being located between the body and the reduced section, and wherein the reduced section comprises a bend to shorten a lateral distance between the spinal rod and the neighboring spinal rod.
110. The implant system of claim 101 wherein the fixation component further comprises a substantially U-shaped indentation along a bottom portion of the body oriented substantially perpendicular to a longitudinal axis of the body, and wherein the indentation is adapted to receive a portion of the spinal rod.
111. The implant system of claim 101 wherein the cavity comprises a front section and a rear section, and wherein the connector is positionable within the front section, and wherein the fixation device is positionable within the rear section.
112. The implant system of claim 101 wherein the head is positioned within the cavity such that the fixation device is rotatable along a longitudinal axis of the body.
113. The implant system of claim 101 wherein the fixation device is adapted to be rotatable within the body along a longitudinal axis of the body, and wherein the connector is positionable within the cavity such that the rotation of the fixation device is inhibited.
114. The implant system of claim 101 wherein the fixation component further comprises a pin, and wherein the head is semi-spherical, and wherein the head includes a borehole positioned equidistant from any position along an outer surface of the head, and wherein the pin is positionable within the borehole and the body such that the fixation device is rotatable about the pin along a longitudinal axis of the body, and wherein the pin is adapted to inhibit the fixation device from rotating along an axis perpendicular to a longitudinal axis of the body.
115. The implant system of claim 101 wherein the fixation component further comprises a pin, and wherein the head is semi-spherical, and wherein the head comprises at least two flat edges oriented on substantially opposing sides of the head, and wherein the head includes a borehole positioned equidistant from any position along an outer surface of the head, and wherein the pin is positionable within the borehole and the body such that the fixation device is rotatable about the pin along a longitudinal axis of the body, and wherein the flat edges of the head are positioned within the body such that the flat edges inhibit rotation of the fixation device along an axis perpendicular to the longitudinal axis of the body.
116. An implant system for fixation of the human spine, comprising:
a connector comprising a receiving end forming a substantially U-shaped borehole having an open end;
a spinal rod axially positionable through the open end into the borehole during use, the spinal rod being fixable within the borehole by a clamping force exerted by the connector; and
a fixation component comprising a fixation device and a body, the fixation device comprising a head, the body comprising a cavity, and wherein a portion of the head is positioned within the cavity such that the fixation device may rotate along a longitudinal axis of the body; and
wherein the connector is adapted to be at least partially disposed within the cavity such that a portion of the cavity and the head engage and exert a compressive force onto an outer surface of the receiving end to maintain the spinal rod within the borehole during use, and wherein the compressive force inhibits further rotation of the fixation device during use.
117. The implant system of claim 116 wherein the receiving end comprises a first arm having a first tip and a second arm having a second tip, the first arm and the second arm together forming the substantially U-shaped borehole, and wherein an opening is defined between the first tip and the second tip, and wherein the opening has a width that is adjustable by moving the connector within the cavity.
118. The implant system of claim 116 wherein the cavity further comprises a rear section, and wherein the body further comprises a width, a first section, a second section, and a rear side, and wherein the width is defined by the rear side of the body and an interior surface of the rear section, and wherein the width becomes narrower in a direction from the first section toward the second section of the body, and wherein the interior surface and the fixation device are adapted to concurrently engage separate portions of the receiving end and impart a compressive force against the receiving end to fixably secure the spinal rod within the borehole.
119. The implant system of claim 116 wherein the receiving end further comprises a first arm having a first tip and a second arm having a second tip, the first arm and the second arm together forming the substantially U-shaped borehole, and further comprising a slot in the connector between the receiving end and the fastening end, the slot enabling the first arm and the second arm to be deflected relative to one another, the deflection of the arms causing a change in a distance between the first tip and the second tip.
120. The implant system of claim 116 wherein the fixation component further comprises a bore, and further comprising a locking element adapted to extend through the bore and contact the connector to inhibit movement of the connector within the cavity.
121. The implant system of claim 116 wherein the fixation device is adapted to attach the spinal rod to a vertebra.
122. The implant system of claim 116 wherein the spinal rod comprises a circumferential portion, and wherein greater than about π radians and less than about 2π radians of the circumferential portion is engaged by the receiving end.
123. The implant system of claim 116 wherein the fixation device is a transverse connector for connecting the spinal rod to a neighboring spinal rod, the transverse connector comprising a reduced section and a beveled section, the reduced section having a width less than a width of the body, the beveled section being located between the body and the reduced section, and wherein the reduced section comprises a bend to shorten a lateral distance between the spinal rod and the neighboring spinal rod.
124. The implant system of claim 116 wherein the spinal rod comprises a diameter, and wherein the open end has a width defined by the first tip and the second tip, and wherein the width is adjustable by moving the connector within the cavity.
125. The implant system of claim 116 wherein the fixation component further comprises a substantially U-shaped indentation along a bottom portion of the body oriented substantially perpendicular to a longitudinal axis of the body, and wherein the indentation is adapted to receive a portion of the spinal rod.
126. The implant system of claim 116 wherein the cavity comprises a front section and a rear section, and wherein the fixation device is positionable within the front section, and wherein the connector is positionable within the rear section.
127. The implant system of claim 116 wherein the fixation component further comprises a pin, and wherein the head is semi-spherical, the head defining a borehole positioned equidistant from any position along an outer surface of the head, and wherein the pin is positionable within the borehole and the body such that the fixation device is rotatable about the pin along a longitudinal axis of the body, and wherein the pin is adapted to inhibit rotation of the fixation member along an axis perpendicular to a longitudinal axis of the body.
128. The implant system of claim 116 wherein the fixation component further comprises a pin, and wherein the head is semi-spherical, the head comprising at least two flat edges oriented on substantially opposing sides of the head, and wherein the head defines a borehole positioned equidistant from any position along an outer surface of the head, and wherein the pin is positionable within the borehole and the body such that the fixation device is rotatable about the pin along a longitudinal axis of the body, and wherein the flat edges of the head are positioned within the body such that the flat edges inhibit rotation along an axis perpendicular to the longitudinal axis of the body.
129. The implant system of claim 116 wherein the connector is positionable with the tapered cavity such that the connector lies in between the body and the fixation device.
130. The implant system of claim 116 wherein the connector further comprises a slot extending adjacent to the receiving end, and wherein movement of the receiving end between the cavity and the fixation device causes deflection of the first arm and the second arm such that a portion of the slot narrows and the arms exert a compressive force against the spinal rod to clamp the spinal rod within the borehole.
131. An implant system for fixation of the human spine, comprising:
a connector comprising a receiving end and a lower section defining an opening;
a spinal rod axially positionable through the opening during use such that the opening substantially surrounds the circumferential portion of the spinal rod, the spinal rod being fixable within the opening by a clamping force exerted by the connector; and
a fixation component comprising a fixation device and a body, the fixture device comprising a head, the body comprising a cavity, and wherein a portion of the head is positioned within the cavity; and
wherein the connector is adapted to be at least partially disposed within the cavity such that a portion of the cavity and the head engage and exert a compressive force onto an outer surface of a receiving end to maintain the spinal rod with the borehole during use.
132. The implant system of claim 131 wherein the opening has a width, and wherein the width is adjustable by moving the connector within the cavity.
133. The implant system of claim 131 wherein the connector further comprises a slot communicating with the opening, and wherein the opening has a width that is adjustable by varying the width of the slot.
134. The implant system of claim 131 wherein the connector further comprises a slot communicating with the opening, and wherein the width of the slot is adjustable by varying the position of the connector within the cavity, and wherein the opening has a width that is adjustable by varying the width of the slot.
135. The implant system of claim 131 wherein the cavity comprises a first end and a second end, the distance between the wall of the cavity and the fixation device being narrower at a location proximate the second end than at a location proximate the first end, and wherein the connector further comprises a slot communicating with the opening such that movement of the connector in a direction from the first end to the second end causes a portion of the slot to narrow such that the lower section exerts a compressive force against the spinal rod to clamp the spinal rod within the opening.
136. The implant system of claim 131 wherein the cavity further comprises a rear section, and wherein the body farther comprises a width, a first section, a second section, and a rear side, and wherein the width is defined by the rear side of the body and an interior surface of the rear section, and wherein the width becomes narrower in a direction from the first section toward the second section of the body, and wherein the interior surface and the fixation device are adapted to concurrently engage separate portions of the connector and impart a compressive force against the connector to fixably secure the spinal rod within the opening.
137. The implant system of claim 131 wherein the fixation component further comprises a bore, and further comprising a locking element adapted to extend through the bore and contact the connector to inhibit movement of the connector within the tapered cavity.
138. The implant system of claim 131 wherein the fixation device attaches the spinal rod to a vertebra.
139. The implant system of claim 131 wherein the fixation component further comprises a substantially U-shaped indentation along a bottom portion of the body oriented substantially perpendicular to a longitudinal axis of the body, and wherein the indentation is adapted to receive a portion of the spinal rod.
140. The implant system of claim 131 wherein the cavity comprises a front section and a rear section, and wherein the connector is positionable within the front section, and wherein the fixation device is positionable within the rear section.
141. The implant system of claim 131 wherein the head is positioned within the cavity such that the fixation device is rotatable along a longitudinal axis of the body.
142. The implant system of claim 131 wherein the fixation device is adapted to be rotatable within the body along a longitudinal axis of the body, and wherein the connector is positionable within the cavity such that the rotation of the fixation device is inhibited.
143. The implant system of claim 131 wherein the fixation component further comprises a pin, and wherein the head is semi-spherical, and wherein the head includes a borehole positioned equidistant from any position along an outer surface of the head, and wherein the pin is positionable within the borehole and the body such that the fixation device is rotatable about the pin along a longitudinal axis of the body, and wherein the pin is adapted to inhibit rotation of the fixation member along an axis perpendicular to a longitudinal axis of the body.
144. The implant system of claim 131 wherein the fixation component further comprises a pin, and wherein the head is semi-spherical, and wherein the head comprises at least two flat edges oriented on substantially opposing sides of the head, and wherein the head includes a borehole positioned equidistant from any position along an outer surface of the head, and wherein the pin is positionable within the borehole and the body such that the fixation device is rotatable about the pin along a longitudinal axis of the body, and wherein the flat edges of the head are positioned within the body such that the flat edges inhibit rotation of the fixation device along an axis perpendicular to the longitudinal axis of the body.
145. An implant system for fixation of the human spine, comprising:
a connector comprising a receiving end and a lower section defining an opening;
a spinal rod axially positionable through the opening during use such that the opening substantially surrounds the circumferential portion of the spinal rod, the spinal rod being fixable within the opening by a clamping force exerted by the connector; and
a fixation component comprising a fixation device and a body, the fixation device comprising a head, the body comprising a cavity, and wherein a portion of the head is positioned within the cavity such that the fixation device may rotate along a longitudinal axis of the body; and
wherein the connector is adapted to be at least partially disposed within the cavity such that a portion of the cavity and the head engage and exert a compressive force onto an outer surface of the receiving end to maintain the spinal rod within the opening during use, and wherein the compressive force inhibits further rotation of the fixation device during use.
146. The implant system of claim 145 wherein the opening has a width, and wherein the width is adjustable by moving the connector within the cavity.
147. The implant system of claim 145 wherein the connector further comprises a slot communicating with the opening, and wherein the opening has a width that is adjustable by varying the width of the slot.
148. The implant system of claim 145 wherein the connector further comprises a slot communicating with the opening, and wherein the width of the slot is adjustable by varying the position of the connector within the cavity, and wherein the opening has a width that is adjustable by varying the width of the slot.
149. The implant system of claim 145 wherein the cavity comprises a first end and a second end, the distance between the wall of the cavity and the fixation device being narrower at a location proximate the second end than at a location proximate the first end, and wherein the connector farther comprises a slot communicating with the opening such that movement of the connector in a direction from the first end to the second end causes a portion of the slot to narrow such that the lower section exerts a compressive force against the spinal rod to clamp the spinal rod within the opening.
150. The implant system of claim 145 wherein the cavity further comprises a rear section, and wherein the body farther comprises a width, a first section, a second section, and a rear side, and wherein the width is defined by the rear side of the body and an interior surface of the rear section, and wherein the width becomes narrower in a direction from the first section toward the second section of the body, and wherein the interior surface and the fixation device are adapted to concurrently engage separate portions of the connector and impart a compressive force against the connector to fixably secure the spinal rod within the opening.
151. The implant system of claim 145 wherein the fixation component further comprises a bore, and further comprising a locking element adapted to extend through the bore and contact the connector to inhibit movement of the connector within the tapered cavity.
152. The implant system of claim 145 wherein the fixation device attaches the spinal rod to a vertebra.
153. The implant system of claim 145 wherein the fixation component further comprises a substantially U-shaped indentation along a bottom portion of the body oriented substantially perpendicular to a longitudinal axis of the body, and wherein the indentation is adapted to receive a portion of the spinal rod.
154. The implant system of claim 145 wherein the cavity comprises a front section and a rear section, and wherein the fixation device is positionable within the front section, and wherein the connector is positionable within the rear section.
155. The implant system of claim 145 wherein the fixation component further comprises a pin, and wherein the head is semi-spherical, the head defining a borehole positioned equidistant from any position along an outer surface of the head, and wherein the pin is positionable within the borehole and the body such that the fixation device is rotatable about the pin along a longitudinal axis of the body, and wherein the pin is adapted to inhibit rotation of the fixation member along an axis perpendicular to a longitudinal axis of the body.
156. The implant system of claim 145 wherein the fixation component further comprises a pin, and wherein the head is semi-spherical, the head comprising at least two flat edges oriented on substantially opposing sides of the head, and wherein the head defines a borehole positioned equidistant from any position along an outer surface of the head, and wherein the pin is positionable within the borehole and the body such that the fixation device is rotatable about the pin along a longitudinal axis of the body, and wherein the flat edges of the head are positioned within the body such that the flat edges inhibit rotation along an axis perpendicular to the longitudinal axis of the body.
157. A fixation component for a spinal implant system comprising:
a fixation device comprising a head; and
a body comprising a cavity;
and wherein a portion of the head is positioned within the cavity such that the fixation device may rotate along a longitudinal axis of the body and wherein a connector is adapted to be at least partially disposed within the cavity such that a portion of the cavity and the head engage and exert a compressive force onto an outer surface of the connector to maintain the spinal rod within the opening during use, and wherein the compressive force inhibits further rotation of the fixation device during use.
158. The fixation component of claim 157 further comprising a substantially U-shaped indentation along a bottom portion of the body oriented substantially perpendicular to a longitudinal axis of the body, and wherein the indentation is adapted to receive a portion of the spinal rod.
159. The fixation component of claim 157 wherein the cavity comprises a front section and a rear section, and wherein the fixation device is positionable within the front section, and wherein a connector is positionable within the rear section.
160. The fixation component of claim 157 wherein the head is semi-spherical, and wherein a portion of the head is positioned within the cavity.
161. The fixation component of claim 157 further comprising a pin, and wherein the head is semi-spherical, the head defining a borehole positioned equidistant from any position along an outer surface of the head, and wherein the pin is positionable within the borehole and the body such that the fixation device is rotatable about the pin along a longitudinal axis of the body, and wherein the pin is adapted to inhibit rotation of the fixation device along an axis perpendicular to a longitudinal axis of the body.
162. The fixation component of claim 157 further comprising a pin, and wherein the head is semi-spherical, the head comprising at least two flat edges oriented on substantially opposing sides of the head, and wherein the head defines a borehole positioned equidistant from any position along an outer surface of the head, and wherein the pin is positionable within the borehole and the body such that the fixation device is rotatable about the pin along a longitudinal axis of the body, and wherein the flat edges of the head are positioned within the body such that the flat edges inhibit rotation along an axis perpendicular to the longitudinal axis of the body.
163. A method of surgically implanting a spinal fixation system comprising:
connecting a fixation component to a portion of a spine, the fixation component comprising a body, and a fastening end the body comprising a cavity having an inner surface;
positioning a connector within the cavity, the connector comprising a receiving end having an opening with an open end that is configured to accept a spinal rod, and wherein the connector is positioned within the cavity such that the inner surface of the cavity engages an outer surface of the receiving end;
snapping a spinal rod into the opening through the open end;
tightening a fastener on the fastening end to translate a sleeve, the sleeve comprising a locking surface that imparts a force against the spinal rod to move the connector within the cavity; and
moving the connector within the cavity to translate the sleeve along the body of the fixation component and cause the inner surface of the cavity to exert a compressive force onto the outer surface of the receiving end such that the receiving end is clamped onto the spinal rod to maintain the spinal rod within the opening.
164. The method of claim 163 wherein the cavity is a tapered cavity having a first end and a second end, the tapered cavity narrowing in a direction from the first end to the second end, and wherein moving the connector within the tapered cavity in a direction from the first end to the second end causes the tapered cavity to exert a compressive force against the receiving end to deflect the receiving end and cause the receiving end to clamp the spinal rod within the opening.
165. The method of claim 163, further comprising snapping the connector to the spinal rod after attaching the spinal rod to the spine.
166. The method of claim 163, further comprising snapping a second connector onto the spinal rod after the spinal rod has been attached to the spine, wherein the second connector is placed on the spinal rod without removing the connector from the spinal rod.
167. The method of claim 166, further comprising placing the second connector in a cavity of a second fixation component.
168. The method of claim 163 wherein a portion of the spinal rod extends from the open end of the opening when the rod is snapped into the opening.
169. The method of claim 163 wherein the spinal rod comprises a circumferential portion, and wherein the receiving end surrounds greater than about π radians of the circumferential portion and less than about 2π radians of the circumferential portion after the spinal rod is snapped into the opening.
170. The method of claim 163, further comprising releasing the connector from the cavity, applying a distraction force to the connector, moving the connector to a new position, placing the connector in the cavity; and affixing the connector to the spinal rod and to the fixation component.
171. The method of claim 163 wherein the fixation component is attached to the spine portion with a bone screw, and further comprising pivoting the bone screw about the spinal rod to form an oblique angle between the bone screw and a longitudinal axis of the spinal rod.
172. The method of claim 163, further comprising releasing the connector from the fixation component, distracting the connector to enlarge the opening, and removing the connector from the spinal rod without detaching the spinal rod from the spine.
173. The method of claim 163, wherein the connector is positioned within the cavity and the fixation component is connected to the spine portion before the spinal rod is snapped into the opening.
174. The method of claim 163 wherein moving the connector within the cavity comprises compressing the fixation component and the connector together with a tool.
175. The method of claim 163 wherein the fixation component comprises a fastening end, and wherein moving the connector within the cavity comprises tightening a fastener located on the fastening end.
176. The method of claim 163 wherein the fastening end is threaded and wherein moving the connector within the cavity comprises tightening a nut located on the fastening end.
177. The method of claim 163 wherein the fixation component further comprises a fixation device for attaching the spinal rod to a vertebra.
178. An implant system for fixation of the human spine, comprising:
a connector comprising an opening;
a spinal rod axially positionable through the opening during use such that the opening surrounds a portion of a circumference of the spinal rod, the spinal rod being fixable within the opening by a clamping force exerted by the connector;
a fixation component comprising a body and a fixation device, wherein the body comprises teeth and a cavity, wherein the connector is adapted to be at least partially disposed within the cavity, and wherein the fixation device couples the spinal rod to a vertebra; and
a spacer having teeth configured to engage teeth of the fixation component to inhibit rotation of the spacer relative to the fixation component and a passage, wherein the connector is positioned within the passage, and wherein the spacer is coupled to the connector such that the spacer compresses the opening to fix the spinal rod to the connector.
179. The implant system of claim 178 wherein the opening has a width, and wherein the width is adjustable by moving the connector within the cavity.
180. The implant system of claim 178 wherein the connector further comprises a slot communicating with the opening, and wherein the opening has a width that is adjustable by varying the width of the slot.
181. The implant system of claim 178 wherein the connector further comprises a slot communicating with the opening, and wherein the width of the slot is adjustable by varying the position of the connector within the cavity.
182. The implant system of claim 178 wherein the passage comprises a first end and a second end, the passage being narrower at a location proximate the second end than at a location proximate the first end, and wherein the connector further comprises a slot communicating with the opening such that movement of the connector in a direction from the first end to the second end causes a portion of the slot to narrow such that the connector exerts a compressive force against the spinal rod to clamp the spinal rod within the opening.
183. The implant system of claim 178 wherein the passage of the body is a tapered passage having a first end and a second end, and wherein the tapered passage narrows in a direction from the first end to the second end, and wherein the tapered passage is adapted to substantially surround a portion of the connector and impart a compressive force against the connector to fixably secure the spinal rod within the opening.
184. The implant system of claim 178 further comprising a nut, wherein the nut is configured to engage threading on the connector to fix a position of the connector relative to the fixation component.
185. The implant system of claim 178 further comprising a nut, wherein the nut is configured to engage threading on the connector, and wherein rotating the nut in a first direction moves the connector into the passage and causes the connector to compress against the spinal rod.
186. The implant system of claim 178 wherein the passage is a tapered cavity, and wherein the outer surface of the connector has a taper that complements that of the tapered passage, and wherein the connector is adapted to be moved within the tapered passage such that an inner surface that defines the tapered passage exerts a compressive force against the outer surface of the connector to clamp the spinal rod within the opening, the compressive force having a magnitude that is a function of a distance that the connector is moved into the tapered passage.
187. The implant system of claim 178 wherein the body comprises a substantially U-shaped yoke having an axial length, the yoke being formed between a top section and a bottom section, the top section comprising a first edge, the bottom section comprising a second edge, the first and second edges defining a width of the yoke, and wherein the first and second edges are curved such that the width of the yoke varies across the axial length of the yoke.
188. The implant system of claim 178 wherein the body further comprises a top section and a bottom section, the cavity being formed in between the top section and the bottom section, the top section and the bottom section each comprising edges that are curved, and wherein the fixation component is adapted to pivot about the spinal rod in a substantially vertical plane, and wherein the curved edges are adapted to contact the spinal rod during the pivoting of the fixation component, thereby defining a range of pivotal motion of the fixation component.
189. The implant system of claim 178 wherein the system further comprises a transverse connector for connecting the spinal rod to a neighboring spinal rod, the transverse connector comprising a reduced section, the reduced section having a width less than a width of the body, wherein the reduced section is configured to be bent to allow for adjustment of a length of the transverse connector.
190. The implant system of claim 178 wherein the system further comprises a transverse connector for connecting the spinal rod to a neighboring spinal rod, the transverse connector comprising a reduced section, the reduced section having a width less than a width of the body, wherein the reduced section is configured to be bent to allow for adjustment of a first end of the transverse connector relative to a second end of the transverse connector to accommodate an orientation of spinal rods when the spinal rod is not parallel to the neighboring spinal rod.
191. An implant system for fixation of the human spine, comprising:
a connector comprising a receiving end defining an opening with an open end;
a spinal rod axially positionable through the open end into the opening during use, the spinal rod being fixable within the opening by a clamping force exerted by the connector; and
a fixation component comprising a body and a fixation device, wherein the body comprises a cavity having an inner surface, wherein a portion of the fixation component is configured to contact the connector and apply a compressive force onto an outer surface of the receiving end to maintain the spinal rod within the opening, and wherein the fixation device is configured to attach the spinal rod to a vertebra during use.
192. The implant system of claim 191 wherein the fixation component further comprises a fixation device and a spacer adapted to fit between the connector and the fixation component, the fixation device comprising protrusions, the spacer offsetting the fixation device from the spinal rod and comprising teeth adapted to form a complementary engagement with the protrusions to inhibit rotation of the fixation device about the spacer.
193. The implant system of claim 191 wherein moving the connector within the cavity comprises translating a sleeve along the body of the fixation component.
194. The implant system of claim 191 wherein the fixation component comprises a fastening end, and further comprising tightening a fastener on the fastening end to translate a sleeve, the sleeve comprising a locking surface that imparts a force against the spinal rod to move the connector within the cavity.
195. The implant system of claim 191 wherein the connector comprises threading, and further comprising a nut that couples to the threading to fix the connector relative to the fixation component.
196. An implant system for fixation of the human spine, comprising:
a connector comprising a receiving end defining an opening with an open end;
a spinal rod axially positionable through the open end into the opening during use, the spinal rod being fixable within the borehole by a clamping force exerted by the connector;
a fixation component comprising a body, the body comprising an engager and a cavity, and wherein the connector is adapted to be at least partially disposed within the cavity; and
a spacer positionable between the body and the spinal rod, the spacer having an engager configured to interact with the engager of the body to inhibit rotation of the spacer relative to the fixation component, and a passage configured to contact the connector and allow compression of the connector that fixes a position of the spinal rod relative to the fixation component.
197. The implant system of claim 196 wherein the fixation component further comprises a fixation device for attaching the spinal rod to a vertebra.
198. The implant system of claim 196 wherein the connector comprises threading, and further comprising a nut configured to engage the threading to fix the position of the connector relative to the fixation component.
199. An implant system for fixation of the human spine, comprising:
a connector comprising a receiving end that defines an opening with an open end;
a spinal rod axially positionable through the open end into the opening during use, the spinal rod being fixable within the opening by a clamping force exerted by the connector; and
a fixation component comprising a body and a sleeve, wherein the body comprises a cavity, wherein the connector is adapted to be at least partially disposed within the cavity, wherein the fixation component is configured to contact the connector to generate the clamping force, and wherein the sleeve comprises an opening being adapted to fit the sleeve substantially about the body of the fixation component during use.
200. The implant system of claim 199 wherein the fixation component further comprises a fixation device for attaching the spinal rod to a vertebra.
201. The implant system of claim 199 wherein the fixation component comprises a fastening end, and further comprising tightening a fastener on the fastening end to translate a sleeve, the sleeve comprising a locking surface that imparts a force against the spinal rod to move the connector within the cavity.
202. An implant system for fixation of the human spine, comprising:
a connector comprising a receiving end defining an opening with an open end;
a spinal rod axially positionable through the open end into the opening during use, the spinal rod being fixable within the opening by a clamping force exerted by the connector; and
a fixation component comprising a fastening end, a sleeve and a body having a cavity, wherein the connector is adapted to be at least partially disposed within the cavity so that interaction of the fixation component with the connector generates the clamping force; and
a fastener configured to couple to the fastening end to translate the sleeve, wherein the sleeve imparts a force against the spinal rod and connector that moves the connector within the cavity during use.
203. The implant system of claim 202 wherein the fixation component further comprises a fixation device for attaching the spinal rod to a vertebra.
204. The implant system of claim 202 wherein the fastener comprises a nut.
205. An implant system for fixation of the human spine, comprising:
a connector comprising a lower section and an upper section, the lower section defining an opening, the upper section defining a slot communicating with the opening;
a spinal rod axially positionable in the opening during use such that the opening surrounds a circumferential portion of the spinal rod; and
a fixation component comprising a body, the body comprising a tapered cavity having an inner surface, the tapered cavity being adapted to receive the connector such that the inner surface engages an outer surface of the connector, and a threaded opening;
a screw adapted to extend into the threaded opening and contact the connector to compress the connector against the spinal rod, and to fix the position of the connector relative to the rod and the connector.
206. The implant system of claim 205 wherein the fixation component further comprises a fixation device and a spacer adapted to fit between the connector and the fixation component, the fixation device comprising protrusions, the spacer offsetting the fixation device from the spinal rod and comprising teeth adapted to form a complementary engagement with the protrusions to inhibit rotation of the fixation device about the spacer.
207. The implant system of claim 205 wherein the lower section surrounds greater than π radians and less than 2π radians of a circumference of the spinal rod.
208. An implant system for fixation of the human spine, comprising:
a connector comprising a lower section and an upper section, the lower section defining an opening, the upper section defining a slot communicating with the opening;
a spinal rod axially positionable through the opening such that the opening surrounds a circumferential portion of the spinal rod;
a fixation component comprising a body, the body comprising a tapered cavity having an inner surface, the tapered cavity being adapted to receive the connector such that the inner surface engages an outer surface of the connector, and a fixation device comprising protrusions; and
a spacer offsetting the fixation device from the spinal rod and comprising teeth adapted to form a complementary engagement with the protrusions to inhibit rotation of the fixation device about the spacer during use;
wherein the connector is moveable within the tapered cavity to cause a width of the slot to vary such that a width of the opening is altered, and wherein the lower section exerts a compressive force against the spinal rod to maintain the spinal rod within the opening during use.
209. The implant system of claim 208 wherein the fixation component further comprises a threaded bore, and further comprising a screw adapted to extend through the bore and contact the connector to inhibit movement of the connector within the tapered cavity.
210. The implant system of claim 208 wherein moving the connector within the cavity comprises translating a sleeve along the body of the fixation component.
211. The implant system of claim 208 wherein the lower section surrounds greater than π radians and less than 2π radians of a circumference of the spinal rod.
212. An implant system for fixation of the human spine, comprising:
a connector comprising a lower section and an upper section, the lower section defining an opening, the upper section defining a slot communicating with the opening;
a spinal rod axially positionable through the opening during use such that the lower section surrounds a circumferential portion of the spinal rod;
a fixation component comprising a body, the body comprising a tapered cavity having an inner surface, the tapered cavity being adapted to receive the connector such that the inner surface engages an outer surface of the connector, and a sleeve, wherein the sleeve is adapted to fit substantially about the body of the fixation component during use; and
wherein the connector is moveable within the tapered cavity to cause a width of the slot to vary such that a compressive force is exerted against the spinal rod by the connector to fix the position of the spinal rod relative to the fixation component.
213. The implant system of claim 212 wherein the fixation component comprises a fastening end, and further comprising tightening a fastener on the fastening end to translate a sleeve, the sleeve comprising a locking surface that imparts a force against the spinal rod to move the connector within the cavity.
214. The implant system of claim 212 wherein the lower section surrounds greater than π radians and less than 2π radians of a circumference of the spinal rod.
215. An implant system for fixation of the human spine, comprising:
a connector comprising a lower section and an upper section, the lower section defining an opening, the upper section defining a slot communicating with the opening;
a spinal rod axially positionable through the opening during use such that the lower section surrounds a circumferential portion of the spinal rod; and
a fixation component comprising a body, the body comprising a tapered cavity having an inner surface, the tapered cavity being adapted to receive the connector such that the inner surface engages an outer surface of the connector, and a fastener on a fastening end to translate a sleeve, the sleeve comprising a locking surface that imparts a force against the spinal rod to move the connector within the cavity during use;
and wherein the connector is moveable within the tapered cavity to cause a width of the slot to vary such that a width of the opening is altered, and wherein the lower section exerts a compressive force against the spinal rod to maintain the spinal rod within the opening during use.
216. The implant system of claim 215 wherein the lower section surrounds greater than π radians and less than 2π radians of a circumference of the spinal rod.
217. A method of surgically implanting a spinal fixation system comprising:
connecting a fixation component to a portion of a spine, the fixation component comprising a body and a rotatable fixation device, the body comprising a cavity having an inner surface, the rotatable fixation device being adapted to engage a portion of a spine;
rotating the fixation device to the desired angle with respect to the body;
positioning a connector within the cavity, the connector comprising a receiving end and a lower section that defines an opening, and wherein the connector is positioned within the cavity such that the inner surface of the cavity engages an outer surface of the connector;
positioning a spinal rod through the opening;
moving the connector within the cavity to translate a sleeve along the body of the fixation component and cause the inner surface of the cavity to exert a compressive force onto the outer surface of the receiving end such that the receiving end is clamped onto the spinal rod to maintain the spinal rod within the opening; and
fixing a position of the sleeve relative to the fixation component.
218. The method of claim 217 wherein moving the connector within the cavity comprises compressing the fixation component and the connector together with a tool.
219. The method of claim 217 wherein positioning a spinal rod through the opening comprises snapping the spinal rod into an open end of the lower section.
220. The method of claim 217 wherein fixing the position of the sleeve relative to the fixation component comprises tightening a fastener on a fastening end of the fixation component to translate a sleeve, the sleeve comprising a locking surface that imparts a force against the spinal rod to move the connector within the cavity.
221. The method of claim 217 wherein fixing the position of the sleeve relative to the fixation component comprises threading a screw into a bore to contact an end of the screw against the connector.
222. The method of claim 217 wherein the fixation component further comprises a fixation device for attaching the spinal rod to a vertebra.
223. The method of claim 217 wherein the lower section surrounds greater than π radians and less than 2π radians of a circumference of the spinal rod.
224. A method of surgically implanting a spinal fixation system comprising:
connecting a fixation component to a portion of a spine, the fixation component comprising a body, the body comprising a cavity having an inner surface;
positioning a connector within the cavity, the connector comprising a receiving end and a fastening end, the receiving end forming an opening with an open end, and wherein the connector is positioned within the cavity such that the inner surface of the cavity engages an outer surface of the receiving end;
engaging a fastener with the fastening end;
snapping a spinal rod into the open end of the opening; and
tightening the fastener to clamp the receiving end to the spinal rod.
225. The method of claim 224 wherein moving the connector within the cavity comprises compressing the fixation component and the connector together with a tool.
226. The method of claim 224 wherein moving the connector within the cavity comprises translating a sleeve along the body of the fixation component.
227. The method of claim 224 wherein the fixation component comprises a fastening end, and further comprising tightening a fastener on the fastening end to translate a sleeve, the sleeve comprising a locking surface that imparts a force against the spinal rod to move the connector within the cavity.
228. The method of claim 224 wherein the fixation component further comprises a threaded bore, and further comprising a screw adapted to extend through the bore and contact the connector to inhibit movement of the connector within the tapered cavity.
229. The method of claim 224 wherein the fixation component further comprises a fixation device for attaching the spinal rod to a vertebra.
230. The method of claim 224 wherein the fixation component further comprises a fixation device and a spacer adapted to fit between the connector and the fixation device, the fixation device comprising protrusions, the spacer offsetting the fixation device from the spinal rod and comprising teeth adapted to form a complementary engagement with the protrusions to inhibit rotation of the fixation device about the spacer.
231. The method of claim 224 wherein the lower section surrounds greater than π radians and less than 2π radians of a circumference of the spinal rod.
232. A method of surgically implanting a spinal fixation system comprising:
connecting a fixation component to a portion of a spine, the fixation component comprising a fastening end and a body with a cavity;
positioning a connector within the cavity, the connector comprising a receiving end that forms an opening;
placing a spinal rod through the opening; and
tightening a fastener on the fastening end to translate a sleeve, the sleeve comprising a locking surface that imparts a force against the spinal rod to move the connector within the cavity.
233. The method of claim 232 wherein moving the connector within the cavity comprises compressing the fixation component and the connector together with a tool.
234. The method of claim 232 wherein moving the connector within the cavity comprises translating a sleeve along the body of the fixation component.
235. The method of claim 232 wherein the fixation component further comprises a fixation device for attaching the spinal rod to a vertebra.
236. The method of claim 232 wherein the receiving end surrounds greater than π radians and less than 2π radians of a circumference of the spinal rod.
Patent Citations (256)
| Patent | Date | Inventor | Cited By |
|---|---|---|---|
| US4401112(A) | 1983-08-01 | Rezaian | Applicant |
| US4433677(A) | 1984-02-01 | Ulrich et al. | Applicant |
| US4492226(A) | 1985-01-01 | Belykh et al. | Applicant |
| US4501269(A) | 1985-02-01 | Bagby | Applicant |
| US4503848(A) | 1985-03-01 | Caspar et al. | Applicant |
| US4570618(A) | 1986-02-01 | Wu | Applicant |
| US4604995(A) | 1986-08-01 | Stephens et al. | Applicant |
| US4641636(A) | 1987-02-01 | Cotrel | Applicant |
| US4643178(A) | 1987-02-01 | Nastari et al. | Applicant |
| US4743256(A) | 1988-05-01 | Brantigan | Applicant |
| US4763644(A) | 1988-08-01 | Webb | Applicant |
| US4805602(A) | 1989-02-01 | Puno et al. | Applicant |
| US4834757(A) | 1989-05-01 | Brantigan | Applicant |
| US4878915(A) | 1989-11-01 | Brantigan | Applicant |
| US4887596(A) | 1989-12-01 | Sherman | Applicant |
| US4946458(A) | 1990-08-01 | Herma et al. | Applicant |
| US4950269(A) | 1990-08-01 | Gaines, Jr. | Applicant |
| US4961740(A) | 1990-10-01 | Ray et al. | Applicant |
| US4966600(A) | 1990-10-01 | Songer et al. | Applicant |
| US4987892(A) | 1991-01-01 | Krag et al. | Applicant |
| US5005562(A) | 1991-04-01 | Cotrel | Applicant |
| US5026373(A) | 1991-06-01 | Ray et al. | Applicant |
| US5047029(A) | 1991-09-01 | Aebi et al. | Applicant |
| US5055104(A) | 1991-10-01 | Ray | Applicant |
| US5074864(A) | 1991-12-01 | Cozad et al. | Applicant |
| US5102412(A) | 1992-04-01 | Rogozinski | Applicant |
| US5108399(A) | 1992-04-01 | Eitenmuller et al. | Applicant |
| US5108446(A) | 1992-04-01 | Wagner et al. | Applicant |
| US5116340(A) | 1992-05-01 | Songer et al. | Applicant |
| US5123926(A) | 1992-06-01 | Pisharodi | Applicant |
| US5127912(A) | 1992-07-01 | Ray et al. | Applicant |
| US5129388(A) | 1992-07-01 | Vignaud et al. | Applicant |
| US5129904(A) | 1992-07-01 | Illi | Applicant |
| US5147359(A) | 1992-09-01 | Cozad et al. | Applicant |
| US5154718(A) | 1992-10-01 | Cozad et al. | Applicant |
| US5171278(A) | 1992-12-01 | Pisharodi | Applicant |
| US5176678(A) | 1993-01-01 | Tsou | Applicant |
| US5176680(A) | 1993-01-01 | Vignaud et al. | Applicant |
| US5181917(A) | 1993-01-01 | Rogozinski | Applicant |
| US5192321(A) | 1993-03-01 | Strokon | Applicant |
| US5192327(A) | 1993-03-01 | Brantigan et al. | Applicant |
| US5201734(A) | 1993-04-01 | Cozad et al. | Applicant |
| US5242445(A) | 1993-09-01 | Ashman | Applicant |
| US5242448(A) | 1993-09-01 | Pettine et al. | Applicant |
| US5246442(A) | 1993-09-01 | Ashman et al. | Applicant |
| US5261909(A) | 1993-11-01 | Sutterlin et al. | Applicant |
| US5263953(A) | 1993-11-01 | Bagby | Applicant |
| US5281222(A) | 1994-01-01 | Allard et al. | Applicant |
| US5282801(A) | 1994-02-01 | Sherman | Applicant |
| US5290312(A) | 1994-03-01 | Kojimoto et al. | Applicant |
| US5290494(A) | 1994-03-01 | Coombes et al. | Applicant |
| US5303718(A) | 1994-04-01 | Krajicek | Applicant |
| US5304179(A) | 1994-04-01 | Wagner | Applicant |
| US5306307(A) | 1994-04-01 | Senter et al. | Applicant |
| US5306309(A) | 1994-04-01 | Wagner et al. | Applicant |
| US5312405(A) | 1994-05-01 | Korotko et al. | Applicant |
| US5312410(A) | 1994-05-01 | Miller et al. | Applicant |
| US5318566(A) | 1994-06-01 | Miller et al. | Applicant |
| US5336223(A) | 1994-08-01 | Rogers | Applicant |
| US5336240(A) | 1994-08-01 | Metzler et al. | Applicant |
| US5344422(A) | 1994-09-01 | Frigg | Applicant |
| US5348026(A) | 1994-09-01 | Davidson | Applicant |
| US5357983(A) | 1994-10-01 | Mathews | Applicant |
| US5360429(A) | 1994-11-01 | Jeanson et al. | Applicant |
| US5360431(A) | 1994-11-01 | Puno et al. | Applicant |
| US5361766(A) | 1994-11-01 | Nichols et al. | Applicant |
| US5364399(A) | 1994-11-01 | Lowery et al. | Applicant |
| US5368594(A) | 1994-11-01 | Martin et al. | Applicant |
| US5380325(A) | 1995-01-01 | Lahille et al. | Applicant |
| US5385583(A) | 1995-01-01 | Cotrel | Applicant |
| US5390683(A) | 1995-02-01 | Pisharodi | Applicant |
| US5395374(A) | 1995-03-01 | Miller et al. | Applicant |
| US5397364(A) | 1995-03-01 | Kozak et al. | Applicant |
| US5403315(A) | 1995-04-01 | Ashman | Applicant |
| US5405391(A) | 1995-04-01 | Hednerson et al. | Applicant |
| US5415658(A) | 1995-05-01 | Kilpela et al. | Applicant |
| US5417690(A) | 1995-05-01 | Sennett et al. | Applicant |
| US5423820(A) | 1995-06-01 | Miller et al. | Applicant |
| US5423825(A) | 1995-06-01 | Levine | Applicant |
| US5425772(A) | 1995-06-01 | Brantigan | Applicant |
| US5437669(A) | 1995-08-01 | Yuan et al. | Applicant |
| US5466237(A) | 1995-11-01 | Byrd, III et al. | Applicant |
| US5474555(A) | 1995-12-01 | Puno et al. | Applicant |
| US5480437(A) | 1996-01-01 | Draenert | Applicant |
| US5484437(A) | 1996-01-01 | Michelson | Applicant |
| US5489307(A) | 1996-02-01 | Kuslich et al. | Applicant |
| US5489308(A) | 1996-02-01 | Kuslich et al. | Applicant |
| US5496318(A) | 1996-03-01 | Howland et al. | Applicant |
| US5505732(A) | 1996-04-01 | Michelson | Applicant |
| US5507746(A) | 1996-04-01 | Lin | Applicant |
| US5514180(A) | 1996-05-01 | Heggeness et al. | Applicant |
| US5520690(A) | 1996-05-01 | Errico et al. | Applicant |
| US5522899(A) | 1996-06-01 | Michelson | Applicant |
| US5527341(A) | 1996-06-01 | Gogolewski et al. | Applicant |
| US5531746(A) | 1996-07-01 | Errico et al. | Applicant |
| US5531751(A) | 1996-07-01 | Schultheiss et al. | Applicant |
| US5536270(A) | 1996-07-01 | Songer et al. | Applicant |
| US5536271(A) | 1996-07-01 | Daly et al. | Applicant |
| US5545165(A) | 1996-08-01 | Biedermann et al. | Applicant |
| US5549608(A) | 1996-08-01 | Errico et al. | Applicant |
| US5549612(A) | 1996-08-01 | Yapp et al. | Applicant |
| US5554157(A) | 1996-09-01 | Errico et al. | Applicant |
| US5563124(A) | 1996-10-01 | Damien et al. | Applicant |
| US5569246(A) | 1996-10-01 | Ojima et al. | Applicant |
| US5569248(A) | 1996-10-01 | Mathews | Applicant |
| US5569253(A) | 1996-10-01 | Farris et al. | Applicant |
| US5571192(A) | 1996-11-01 | Schönhöffer | Applicant |
| US5575792(A) | 1996-11-01 | Errico et al. | Applicant |
| US5578033(A) | 1996-11-01 | Errico et al. | Applicant |
| US5584834(A) | 1996-12-01 | Errico et al. | Applicant |
| US5586984(A) | 1996-12-01 | Errico et al. | Applicant |
| US5593407(A) | 1997-01-01 | Reis | Applicant |
| US5593409(A) | 1997-01-01 | Michelson | Applicant |
| US5601553(A) | 1997-02-01 | Trebing et al. | Applicant |
| US5601556(A) | 1997-02-01 | Pisharodi | Applicant |
| US5603713(A) | 1997-02-01 | Aust et al. | Applicant |
| US5607424(A) | 1997-03-01 | Tropiano | Applicant |
| US5607425(A) | 1997-03-01 | Rogozinski | Applicant |
| US5607426(A) | 1997-03-01 | Ralph et al. | Applicant |
| US5607430(A) | 1997-03-01 | Bailey | Applicant |
| US5609592(A) | 1997-03-01 | Brumfield et al. | Applicant |
| US5609593(A) | 1997-03-01 | Errico et al. | Applicant |
| US5609594(A) | 1997-03-01 | Errico et al. | Applicant |
| US5609596(A) | 1997-03-01 | Pepper | Applicant |
| US5609635(A) | 1997-03-01 | Michelson | Applicant |
| US5609636(A) | 1997-03-01 | Kohrs et al. | Applicant |
| US5611800(A) | 1997-03-01 | Davis et al. | Applicant |
| US5611801(A) | 1997-03-01 | Songer | Applicant |
| US5613967(A) | 1997-03-01 | Engelhardt et al. | Applicant |
| US5616144(A) | 1997-04-01 | Yapp et al. | Applicant |
| US5620443(A) | 1997-04-01 | Gertzbein et al. | Applicant |
| US5624441(A) | 1997-04-01 | Sherman et al. | Applicant |
| US5626579(A) | 1997-05-01 | Muschler et al. | Applicant |
| US5628740(A) | 1997-05-01 | Mullane | Applicant |
| US5628756(A) | 1997-05-01 | Barker, Jr. et al. | Applicant |
| US5630816(A) | 1997-05-01 | Kambin | Applicant |
| US5632747(A) | 1997-05-01 | Scarborough et al. | Applicant |
| US5634925(A) | 1997-06-01 | Urbanski | Applicant |
| US5643260(A) | 1997-07-01 | Doherty | Applicant |
| US5643264(A) | 1997-07-01 | Sherman et al. | Applicant |
| US5643265(A) | 1997-07-01 | Errico et al. | Applicant |
| US5645084(A) | 1997-07-01 | McKay | Applicant |
| US5645544(A) | 1997-07-01 | Tai et al. | Applicant |
| US5645549(A) | 1997-07-01 | Boyd et al. | Applicant |
| US5645598(A) | 1997-07-01 | Brosnahan, III | Applicant |
| US5647873(A) | 1997-07-01 | Errico et al. | Applicant |
| US5649927(A) | 1997-07-01 | Kilpela et al. | Applicant |
| US5651283(A) | 1997-07-01 | Runciman et al. | Applicant |
| US5651789(A) | 1997-07-01 | Cotrel | Applicant |
| US5653708(A) | 1997-08-01 | Howland | Applicant |
| US5653709(A) | 1997-08-01 | Frigg | Applicant |
| US5653763(A) | 1997-08-01 | Errico et al. | Applicant |
| US5658289(A) | 1997-08-01 | Boucher et al. | Applicant |
| US5658337(A) | 1997-08-01 | Kohrs et al. | Applicant |
| US5658516(A) | 1997-08-01 | Eppley et al. | Applicant |
| US5662651(A) | 1997-09-01 | Tornier et al. | Examiner |
| US5662653(A) | 1997-09-01 | Songer et al. | Applicant |
| US5665088(A) | 1997-09-01 | Gil et al. | Applicant |
| US5665112(A) | 1997-09-01 | Thal | Applicant |
| US5665122(A) | 1997-09-01 | Kambin | Applicant |
| US5667506(A) | 1997-09-01 | Sutterlin | Applicant |
| US5667507(A) | 1997-09-01 | Corin et al. | Applicant |
| US5667508(A) | 1997-09-01 | Errico et al. | Applicant |
| US5668288(A) | 1997-09-01 | Storey et al. | Applicant |
| US5669909(A) | 1997-09-01 | Zdeblick et al. | Applicant |
| US5669910(A) | 1997-09-01 | Korhonen et al. | Applicant |
| US5669911(A) | 1997-09-01 | Errico et al. | Applicant |
| US5671695(A) | 1997-09-01 | Schroeder | Applicant |
| US5672175(A) | 1997-09-01 | Martin | Applicant |
| US5672176(A) | 1997-09-01 | Biedermann et al. | Applicant |
| US5674222(A) | 1997-10-01 | Berger et al. | Applicant |
| US5674295(A) | 1997-10-01 | Ray et al. | Applicant |
| US5674296(A) | 1997-10-01 | Bryan et al. | Applicant |
| US5676665(A) | 1997-10-01 | Bryan | Applicant |
| US5676666(A) | 1997-10-01 | Oxland et al. | Applicant |
| US5676701(A) | 1997-10-01 | Yuan et al. | Applicant |
| US5676703(A) | 1997-10-01 | Gelbard | Applicant |
| US5681311(A) | 1997-10-01 | Foley et al. | Applicant |
| US5681312(A) | 1997-10-01 | Yuan et al. | Applicant |
| US5683292(A) | 1997-11-01 | Richelsoph et al. | Applicant |
| US5683391(A) | 1997-11-01 | Boyd | Applicant |
| US5683393(A) | 1997-11-01 | Ralph | Applicant |
| US5683394(A) | 1997-11-01 | Rinner | Applicant |
| US5688272(A) | 1997-11-01 | Montague et al. | Applicant |
| US5688273(A) | 1997-11-01 | Errico et al. | Applicant |
| US5688274(A) | 1997-11-01 | Errico et al. | Applicant |
| US5688279(A) | 1997-11-01 | McNulty et al. | Applicant |
| US5688280(A) | 1997-11-01 | Booth, Jr. et al. | Applicant |
| US5690629(A) | 1997-11-01 | Asher et al. | Applicant |
| US5690630(A) | 1997-11-01 | Errico et al. | Applicant |
| US5690631(A) | 1997-11-01 | Duncan et al. | Applicant |
| US5690632(A) | 1997-11-01 | Schwartz et al. | Applicant |
| US5690633(A) | 1997-11-01 | Taylor et al. | Applicant |
| US5690842(A) | 1997-11-01 | Panchison | Applicant |
| US5693046(A) | 1997-12-01 | Songer et al. | Applicant |
| US5693053(A) | 1997-12-01 | Estes | Applicant |
| US5693100(A) | 1997-12-01 | Pisharodi | Applicant |
| US5697929(A) | 1997-12-01 | Mellinger | Applicant |
| US5697977(A) | 1997-12-01 | Pisharodi | Applicant |
| US5700291(A) | 1997-12-01 | Kuslich et al. | Applicant |
| US5700292(A) | 1997-12-01 | Margulies | Applicant |
| US5702391(A) | 1997-12-01 | Lin | Applicant |
| US5702392(A) | 1997-12-01 | Wu et al. | Applicant |
| US5702393(A) | 1997-12-01 | Pfaifer | Applicant |
| US5702394(A) | 1997-12-01 | Henry et al. | Applicant |
| US5702395(A) | 1997-12-01 | Hopf | Applicant |
| US5702396(A) | 1997-12-01 | Hoenig et al. | Applicant |
| US5702399(A) | 1997-12-01 | Kilpela et al. | Applicant |
| US5702449(A) | 1997-12-01 | McKay | Applicant |
| US5702450(A) | 1997-12-01 | Bisserie | Applicant |
| US5702451(A) | 1997-12-01 | Biedermann et al. | Applicant |
| US5702452(A) | 1997-12-01 | Argenson et al. | Applicant |
| US5702453(A) | 1997-12-01 | Rabbe et al. | Applicant |
| US5702454(A) | 1997-12-01 | Baumgartner | Applicant |
| US5702455(A) | 1997-12-01 | Saggar | Applicant |
| US5704936(A) | 1998-01-01 | Mazel | Applicant |
| US5704937(A) | 1998-01-01 | Martin | Applicant |
| US5707372(A) | 1998-01-01 | Errico | Applicant |
| US5707395(A) | 1998-01-01 | Li | Applicant |
| US5709681(A) | 1998-01-01 | Pennig | Applicant |
| US5709682(A) | 1998-01-01 | Medoff | Applicant |
| US5709683(A) | 1998-01-01 | Bagby | Applicant |
| US5709684(A) | 1998-01-01 | Errico et al. | Applicant |
| US5709685(A) | 1998-01-01 | Dombrowski et al. | Applicant |
| US5709686(A) | 1998-01-01 | Talos et al. | Applicant |
| US5713841(A) | 1998-02-01 | Graham | Applicant |
| US5713898(A) | 1998-02-01 | Stucker et al. | Applicant |
| US5713899(A) | 1998-02-01 | Marnay et al. | Applicant |
| US5713900(A) | 1998-02-01 | Benzel et al. | Applicant |
| US5713903(A) | 1998-02-01 | Sander et al. | Applicant |
| US5713904(A) | 1998-02-01 | Errico et al. | Applicant |
| US5716355(A) | 1998-02-01 | Jackson | Applicant |
| US5716356(A) | 1998-02-01 | Biedermann et al. | Applicant |
| US5716357(A) | 1998-02-01 | Rogozinski | Applicant |
| US5716358(A) | 1998-02-01 | Ochoa | Applicant |
| US5716359(A) | 1998-02-01 | Ojima et al. | Applicant |
| US5716415(A) | 1998-02-01 | Steffee | Applicant |
| US5716416(A) | 1998-02-01 | Lin | Applicant |
| US5720746(A) | 1998-02-01 | Soubeiran | Applicant |
| US5720747(A) | 1998-02-01 | Burke | Applicant |
| US5720748(A) | 1998-02-01 | Kuslich et al. | Applicant |
| US5720751(A) | 1998-02-01 | Jackson | Applicant |
| US5722977(A) | 1998-03-01 | Wilhelmy | Applicant |
| US5733284(A) | 1998-03-01 | Martin | Applicant |
| US5797911(A) | 1998-08-01 | Sherman et al. | Applicant |
| US5899903(A) | 1999-05-01 | Cotrel | Applicant |
| US5928233(A) | 1999-07-01 | Apfelbaum et al. | Applicant |
| US5989250(A) | 1999-11-01 | Wagner et al. | Applicant |
| US6132430(A) | 2000-10-01 | Wagner | Applicant |
| US6171311(B1) | 2001-01-01 | Richelsoph | Examiner |
| US6416515(B1) | 2002-07-01 | Wagner | Examiner |
| EP578320 | 1994-01-01 | Applicant | |
| EP778007 | 1997-06-01 | Applicant | |
| EP836836 | 1998-04-01 | Applicant | |
| FR2732887 | 1996-10-01 | Applicant | |
| FR2736535 | 1997-01-01 | Applicant |
Non-Patent Literature (47)
- International Search Report PCT/US 97/16971 dated Feb. 6, 1998.Applicant
- Danek Group, Inc. Medical Division Publication entitled, “TSRH Spinal System—Unmatched versatility,” 1992, pp. 1-4.Applicant
- Danek Surgical Technique Manual entitled, “TSRH Spinal Implant System,” Date Unknown, p. 1-16.Applicant
- Danek Surgical Technique Manual entitled, “TSRH Crosslink,” Date Unknown, pp. 1-8.Applicant
- Dickman Curtis A., et al., BNI Quarterly Publication entitled, “Techniques of Screw Fixation of the Cervical Spine,” vol. 9, No. 4, Fall 1993, pp. 27-39.Applicant
- Slone et al., RadioGraphics Publication entitled, “Spinal Fixation,” vol. 13, No. 2, Mar. 1993, pp. 341-356.Applicant
- Synthes Spine Publication entitled, “The Universal Spinal System—Internal Fixation for the Spine,” 1994, pp.1-15.Applicant
- AcroMed Publication entitled, “The ISOLA Spinal System—Versatility, simplicity and minimal profile in the surgical treatment of the spine,” 1994, pp. 1-15.Applicant
- AcroMed Corporation Publication entitled, “ISOLA® Transverse Rod Connectors: Principles and Techniques,” Date Unknown, pp. i, ii, 1-8.Applicant
- Danek Publication entitled, “AXIS—Fixation System,” 1993, pp. 1-6.Applicant
- Synthes Publication entitled, “Small Notched Titanium Reconstruction Plate System,” 1996, pp. 1-6.Applicant
- J. Neurosurg Publication entitled, “Posterior plates in the management of cervical instability: long-term results in 44 patients,” vol. 81, 1994, pp. 341-349.Applicant
- BNI Quarterly Publication entitled, “Lateral Mass Posterior Plating and Facet Fusion for Cervical Spine Instability,” vol. 7, No. 2, 1991, pp. i, ii, 1-12.Applicant
- Beadling, Lee, Orthopedics Today Publication entitled, “FDA Clears Spinal Cages for Interbody Lumbar Fusion,” pp. 1-2.Applicant
- MedPro Month Publication entitled, “Trends in Spine & Disk Surgery,” vol. VI, No. 11-12, pp. 280-284.Applicant
- Surgical Dynamics Ray Threaded Fusion Cage Device Surgical Technique Manual, pp. 1-10.Applicant
- Surgical Dynamics Ray Threaded Fusion Cage, pp. 1-6.Applicant
- AcroMed Publication entitled, “AcroMed Spinal Solutions for Cervical Pathologies,” 07-95, pp. 1-8.Applicant
- Codman Publication entitled, “Sof′ wire Cable System,” 6 pp.Applicant
- Huhn, Stephen L. et al., “Posterior Spinal Osteosynthesis for Cervical Fracture/Dislocation Using a Flexible Multistrand Cable System: Technical Note,” Neurosurgery, vol. 29, No. 6, 1991, pp. 943-946.Applicant
- Dickman, Curtis A. et al., “Wire Fixation for the Cervical Spine: Biomechanical Principles and Surgical Techniques,” BNI Quarterly, vol. 9, No. 4, Fall 1993, pp. 2-16.Applicant
- Publication by AcroMed entitled, “AcroMed Cable System by Songer,” 9/93, 4 pp.Applicant
- M. Aebi, MD, et al., “Treatment of Cervical Spine Injuries with Anterior Plating: Indications, Techniques, and Results,” vol. 16, No. 3S, Mar., 1991 Supplement, pp. S38-S45.Applicant
- Foley, M.D. et al., “Aline Anterior Cervical Plating System,” Smith & Nephew Richards, Inc. Orthopaedics Catalog Information, 9/96, pp. 1-16.Applicant
- Lowery, Gary L., M.D., Ph.D., Sofamor Danek Group, Inc. Publication entitled, “Orion Anterior Cervical Plate System: Surgical Technique,” 1994, pp. 1-24.Applicant
- Apfelbaum, R., M.D., Aesculap Scientific Information publication entitled, “Posterior Transarticular C1-2 Screw Fixation for Atlantoaxial Instability,” 1993, pp. 1-15.Applicant
- Danek Titanium Cable System publication by Danek Group, Inc., 1994, 6 pp.Applicant
- Publication entitled, “Spinal Disorders”, 4 pp.Applicant
- O'Brien, John P., Ph.D., Orthopaedic Product News Article entitled, “Interbody Fusion of the Lumbar Spine,” pp. 1-3.Applicant
- Roy et al., “Variations of Young's Modulus and Hardness in Human Lumbar Vertebrae Measured by Nanoindentation”, pp. 1-4.Applicant
- Sofamor Danek publication entitled, “Atlas Cable System: Evolution of the Cable System for Spinal Applications,” 1995, 2 pp.Applicant
- AcroMed publication entitled, “AcroMed Songer Cable System: Ordering information for Implants and Instruments,” 4/96, 4 pp.Applicant
- Songer, Matthew, M.D., “Acromed Cable System by Songer: Cervical Technique Manual,” pp. 1-17.Applicant
- Songer, Matthew N., M.D., “AcroMed Cable System by Songer: Technique Manual,” 1993, pp. 1-20.Applicant
- Oxland, Thomas R., Ph.D., et al., SpineTech Inc. Publication entitled, “Biomechanical Rationale—The BAK Interbody Fusion System: An Innovative Solution,” pp. 1-16.Applicant
- SpineTech, Inc. publication entitled, “Patient Information on Spinal Fusion Surgery and the BAK Interbody Fusion System,” 10 pp.Applicant
- SpineTech, Inc. publication entitled, “BAK/Cervical Interbody Fusion System,” 1994, 2 pp.Applicant
- SpineTech, Inc. publications entitled, “Instrumentation BAK Interbody Fusion System,” “Biomechanics BAK Interbody Fusion System,” and “Porosity BAK Interbody Fusion System,” 1996, 12 pp.Applicant
- SpineTech, Inc. publication entitled, “The BAK Interbody Fusion System,” 1996, 4 pp.Applicant
- Depuy Motech, Inc. publication entitled, “Moss Miami 3-Dimensional Spinal Instrumentation: Taking Spinal Instrumentation to a New Dimension,” 1995, 8 pp.Applicant
- Shufflebarger, Harry L., M.D., “Moss Miami Instrumentation System: Methods of Fixation of the Spondylopelvic Junction,” Lumbosacral and Spinopelvic Fixation, 1996 by Raven Publishers, Philadelphia, pp. 381-393.Applicant
- Shufflebarger, Harry L., M.D., Depuy Motech publication entitled, “Clinical Issue: Rod Rotation in Scoliosis Surgery,” 5 pp.Applicant
- AcroMed publication entitled, “Instruments,” 3 pp.Applicant
- SpineTech, Inc. publication entitled, “The Bone Harvester,” 1996, 2 pp.Applicant
- Wright Medical Technology Publication entitled, “Versalok Low Back Fixation System,” 1996, pp. 1-4.Applicant
- Danek Medical, Inc. Publication entitled, “TSRH Lumbar System,” 1991, pp. 1-4.Applicant
- Spinal Concepts Inc. publication entitled, “The BacFix ss—Posterior Lower Back Fixation System—Written Surgical Technique,” 1997, pp. 1-11.Applicant