The embodiments in this application are directed generally to medical stabilization implants and methods for implanting those devices, and more particularly to an implantable dynamic connection member with a flexible section coupled between rigid sections to provide selective support to the spine.
A variety of surgical procedures on various parts of the human body can benefit from the use of various implantable stabilization devices. One such area is the human spine which consists of segments known as vertebrae linked by intervertebral disks and held together by ligaments. There are 24 movable vertebrae—7 cervical (neck) vertebrae, 12 thoracic (chest) vertebrae, and 5 lumbar (back) vertebrae. Each vertebra has a somewhat cylindrical bony body (centrum), a number of wing-like projections (processes), and a bony arch. The arches are positioned so that the space they enclose forms the vertebral canal. The vertebral canal houses and protects the spinal cord, and within it the spinal fluid circulates. Ligaments and muscles are attached to various projections of the vertebrae. The bodies of the vertebrae form the supporting column of the skeleton. Fused vertebrae make up the sacrum and coccyx, the very bottom of the vertebral column.
Modern spine surgery often involves the use of spinal stabilization/fixation procedures, for example vertebral body fusion, to correct or treat various spine disorders and/or to support the spine. In conjunction with these procedures, spinal implants may be used to help stabilize the spine, correct deformities of the spine such as spondylolisthesis or pseudoarthrosis, facilitate fusion, treat spinal fractures, or for other purposes. Some spinal implants such as a spinal fixation system may provide fused and/or rigid support for the affected regions of the spine. These spinal stabilization systems often include one or more rods which can bear a portion of the forces that would otherwise be transmitted along the spine. These stabilization rods can be implanted along various regions of the spine and, in some procedures, can be attached to one or more vertebrae of the spine to provide support and stabilize, align, or otherwise treat the region of the spine of interest. The rods can be attached using a variety of anchor systems, including pedicle screws, hooks, cables, and other fixation devices. Examples of pedicle screws and other types of fixation systems and attachments are illustrated in U.S. Pat. Nos. 4,763,644; 4,805,602; 4,887,596; 4,950,269; 5,129,388, 7,073,415, 7,238,204 and 7,166,108, each of which is fully incorporated by reference herein. Spinal fixation systems generally inhibit movement in the affected regions post-implantation.
In some procedures, spinal fixation provides rigid support (i.e., in a fusion procedure) for the affected regions of the spine to severely restrict/limit movement of the affected regions of the spine in virtually all directions. More recently so-called “dynamic” stabilization systems have been introduced wherein the spinal implant allows at least some movement of the affected regions in at least some direction (i.e., flexion, extension, lateral, or torsional movement). In certain circumstances, a dynamic stabilization system can benefit from the use of a stabilization rod that provides some movement in certain directions, while still providing support and stabilization to the overall stabilization system.
Embodiments disclosed herein can be used to stabilize parts of the human body, and in particular, are described in conjunction with providing stabilization of the spine The various embodiments disclosed herein will describe a spinal stabilization rod that can provide dynamic support and/or stabilization of a portion of the spine. As one skilled in the art can appreciate, embodiments of stabilization rods disclosed herein are not limited to dynamic stabilization of the spine and can be applied to and adapted for other surgical applications where providing stabilization or support with some movement is desired.
In one embodiment, a connection member includes a first rigid section, a second rigid section, and a flexible section joined between the first and second rigid sections. In one aspect of this embodiment, the flexible section can be joined to the first and second rigid sections by molding a material to contact connecting portions of each of the first and rigid sections, where the material retains some flexibility relative to the rigid sections post-molding. In some embodiments, the first and second rigid sections are made from a metal, for example titanium, titanium alloys, stainless steel and steel alloys or other suitable rigid materials as would be understood by one of ordinary skill in the art. In some embodiments, the flexible section comprises material with flexibility relative to the rigid sections, for example a moldable material such as polycarbonate urethane or other materials as would be understood by one of ordinary skill in the art.
In another embodiment, the connecting portions of the first and second rigid sections can have an exterior surface where all or a portion of the exterior surface has been adapted to have an increased surface area so as to inhibit separation of the flexible section from the first and second rigid sections. In some embodiments, this increased surface area can constitute an irregular surface made up of a plurality of randomly sized, as defined by height and thickness, and spaced, as defined by proximity there between, protrusions which are substantially unstressed with respect to the exterior surface and which are constructed monolithically therefrom. The connecting portion of the first and second rigid sections can also include one or more features that can further aid in resisting separation of the flexible section from the first and/or second rigid sections. These features can extend radially outward or recess radially inward from the exterior surface of the connecting portions of the first and second rigid sections. In some embodiments, these increased surface area features can include among other features an aperture, an undercut, a protrusion and/or a boss.
In another embodiment, a contact point between the molded material of the flexible section and the first and second rigid sections acts as a barrier against ingress of contaminants between the first/second rigid sections and the flexible section. In some embodiments, the junction between the molded material of the flexible section and the connecting portion of the first rigid section forms this contact point.
In another embodiment, a method of forming a spine stabilization rod is disclosed. In one embodiment, forming a connection member may include forming a first rigid section with a connecting portion having an exterior surface, forming a second rigid section with a connecting portion having an exterior surface, wherein at least a portion of these exterior surfaces are have an increased surface area, and molding a material about the connecting portion of the first rigid section and the connecting portion of the second rigid section to form a flexible section. In one embodiment, the method can include forming an irregular surface on the exterior of the connecting portions of the first and/or second rigid section. In one embodiment, forming the irregular exterior surface can be accomplished as follows: masking the exterior surface in a random pattern with a maskant material so that less than the entire surface portion is covered thereby, etching (for example electrochemically) the surface portion such that material from the first and second rigid section is removed in areas uncovered by the maskant material and areas covered by the maskant material are left intact, removing the maskant material, and repeating the masking, etching and removing steps upon the surface portion until a desired surface irregularity is achieved.
In another embodiment, a spine stabilization system can include a connection member as described above, and two or more anchoring systems for affixing the connection member to two or more vertebrae.
Other features, advantages, and objects of the disclosure will be better appreciated and understood when considered in conjunction with the following description and the accompanying drawings.
A more complete understanding of the present disclosure and the advantages thereof may be acquired by referring to the following description, taken in conjunction with the accompanying drawings in which like reference numbers indicate like features and wherein:
The disclosure and the various features and advantageous details thereof are explained more fully with reference to the non-limiting embodiments detailed in the following description. Descriptions of well known starting materials, manufacturing techniques, components and equipment are omitted so as not to unnecessarily obscure the disclosure in detail. Skilled artisans should understand, however, that the detailed description and the specific examples, while disclosing preferred embodiments of the disclosure, are given by way of illustration only and not by way of limitation. Various substitutions, modifications, and additions within the scope of the underlying inventive concept(s) will become apparent to those skilled in the art after reading this disclosure. Skilled artisans can also appreciate that the drawings disclosed herein are not necessarily drawn to scale.
Surgical approaches used to stabilize the spine include spinal fusion and non-fusion treatment options. Spinal fusion, in simplest terms, is a surgical method for removing the damaged intervertebral disc and growing bone structures together to create a solid bone bridge between vertebrae. A fusion of the spine can be done by way of various known methods. The ideal technique in a particular patient will depend upon a number of factors including, but not limited to, the level(s) of vertebrae to be fused, degree of instability or deformity of the spine, age of the patient, risk factors for non-union (i.e., failure to fuse properly), and experience of the surgeon. Known spinal fusions include anterior spinal fusion, posterior spinal fusion with spinal instrumentation, posterior spinal fusion without spinal instrumentation, circumferential fusion (anterior and posterior), posterior lumbar interbody fusion, and transforaminal lumbar interbody fusion. The last two spinal fusion techniques are less invasive than the circumferential fusion and may decrease complications related to open exposures (e.g., infection, wound healing problems, etc.).
One method of stabilizing a portion of the spine may include coupling a connection member to the spine. Various embodiments are disclosed for a connection member that can include at least one flexible section coupled between two rigid sections, where the flexible section is flexible relative to the rigid sections. In one embodiment, a connection member may be a spine stabilization rod. In a spine stabilization system, the rigid sections of the spine stabilization rod may be coupled to an anchoring device, such as a bone fastener, and, in some embodiments, the flexible section can be aligned with a damaged disk or other portion of the spine that needs stabilization. The flexible section could have varying degrees of flexibility with respect to the rigid sections.
The materials used for rigid sections 201 and 203 and the material used for flexible section 202 may be selected so that a significant amount of flexion or extension is allowed by connection member 30 and/or flexible section 202. In some embodiments, the amount of flexion provided by connection member 30 or flexible section 202 may be approximately 0.1 to 1.0 mm, and in a particular embodiment approximately 0.5 mm, while the amount of extension provided by connection member 30 (or flexible section 202) may be approximately 0.5 mm to 1.5 mm, and in a particular embodiment approximately 1.0 mm. It should be understood that the amount of flexion or extension provided by any particular connection member 30 of the present embodiment can be higher or lower than these numbers, and can be adjusted according to the particular dynamic stabilization need.
In some embodiments, rigid sections 201 and 203 may be made of any biocompatible materials capable of providing a desired rigidity and/or desired modulus of elasticity. In some embodiments, rigid sections 201 and 203 may be manufactured from titanium or a titanium alloy, stainless steel or an alloy, some combination thereof, or some other biocompatible metal. In some embodiments, rigid sections 201 and 203 may be manufactured having a durometer of 55 Shore D or greater. In alternative embodiments, first rigid section 201 and/or second rigid section 203 may be formed from a flexible polymer having a flexibility less than that of flexible section 202. Examples of polymers might include polyethylethylketone (PEEK), polyethylketoneketone (PEKK), and PMMA. Rigid sections 201 and 203 may be of the same or different lengths relative to one another and relative to flexible section 202. For example, in some embodiments, first rigid section 201 may be long enough to span between three vertebrae and second rigid section 203 may be long enough to span between only two vertebrae. In some embodiments, rigid sections 201 and/or 203 may be of a length that allows connection member 30 to be coupled to anchor system 18 (see
As shown in the embodiment of
In alternative embodiments, the cross-sectional profile of connecting portion 223 may increase or decrease along the longitudinal axis of connecting portion 223. While
In various embodiments, connecting portion 223 may be formed to have features extending radially outward or recessing radially inward from an outer surface. These features can include, for example, an aperture, an undercut, a protrusion and/or a boss. These features can increase the surface area for a given length of connecting portions 223, which may improve the connection between rigid section 201 or 203 and flexible section 202. In other words, as compared to a rigid section having a constant diameter and a smooth, continuous surface, a taper, bevel, boss, undercut, aperture, cannula or some other discrete or continuous feature can be used to increase the surface area of connecting portion 223 for a given length of connecting portion 223. For example, as shown in the embodiment of
The embodiments shown in
In some embodiments, once one or more desired features have been formed on connecting portion 223, connecting portion 223 may be exposed to chemical and/or mechanical processes to make the exterior surface 231 (and/or 230) of connecting portion 223 irregular. As illustrated in the embodiments of
Increasing the exterior surface area of connecting portion 223 may include forming a desired surface pattern on connecting portion 223 by removing material from the exterior surface 231 or 230 of connecting portion 223. Etching is one method of removing material to provide an irregular surface. In some embodiments, etching may include the steps of masking a surface portion in a random pattern with a maskant material, such that less than the entire surface portion is covered thereby, electrochemically etching the surface portion such that first rigid section material or second rigid section material is removed thereby in areas uncovered by the maskant material and areas covered by the maskant material are left intact, removing the maskant material, and repeating the masking, electrochemically etching and removing steps upon the surface portion until a desired surface irregularity is achieved.
In one embodiment, chemical etching can be employed to create an irregular exterior surface for the connecting portion 223 of rigid section 201 and/or 203. For purposes of describing the chemical etching, this description will refer to the use of a rigid section made from a titanium alloy base metal. While titanium represents one embodiment, the rigid section may be formed from a number of other alloys may be utilized. Each of these different alloys will require a different maskant and etchant composition. It is, however, considered to be within the knowledge of a person of ordinary skill in the art to select an appropriate etchant based on the base alloy selected. Furthermore, for the purposes of clarity, certain repetitive elements in the drawings have not been numerically identified for each and every occurrence. For example, a number of maskant points are shown on the surface diagrams. It is considered apparent from the drawings that the maskant points and other surface features of the etched implant are repeated and are readily identifiable without the aid of numeric identification for each feature. Only representative features and maskant points have therefore been identified.
Referring now to
The maskant must be chosen in order to provide a substance which will cling tightly to surface 231 of connecting portion 223 during manipulation of connecting portion 223 and will also remain stable when the etchant solution is applied to the coated portion. The maskant must also be removed with no residue once its function has been accomplished. A particular problem encountered when utilizing maskants is the performance of the maskant at the boundaries of its application. The maskant should produce a sharply defined edge once the etching process has begun and not itself deteriorate during the etching process. This might permit partial degradation of the substrate in a masked area. It should be noted, however, that some deterioration is found in any maskant use and does provide some of the particular surface features of the etched connecting portion 223 described later.
Exterior surface 231 of connecting portion 223 should be relatively clean and grease-free, with all or substantially all of any oxidized material removed before the application of the maskant. This may be accomplished either mechanically, chemically or both. Exterior surface 231 may be cleaned mechanically utilizing a light abrasive blast of aluminum oxide particles or glass beads. Alternatively, blasting with any small solid particle which will not degrade surface 231 is contemplated. A chemical agent such as methanol may be utilized alone or in conjunction with the blasting. Most maskants are sensitive to the condition of the applied surface and both application and removal of the maskant may be affected by improper surface treatment. The maskant can be comprised of a number of materials including neoprene elastomers and isobutylene isoprene copolymers. The particular maskant should be selected based on the type of etchant utilized. For the embodiment described, the maskant is AC-818C, an air-cured, general purpose, peelable coating produced by A.C. Products, Inc. of Placentia, Calif. The maskant is thinned utilizing perchlorethylene to 35-45 seconds utilizing a No. 5 Zahn cup. The maskant, if too thin, may be thickened to this viscosity by evaporation of the carrier. While the maskant is traditionally utilized in the 14-18 second range, it has been found that a thicker version can produce superior results in terms of applying the maskant utilizing manual daubing or spray application techniques. It is to be specifically noted that the maskant is applied in a random spattered fashion allowing only a portion of exterior surface 231 of connecting portion 223 to be coated thereby. A random “polka dot” pattern can be used in which each of the maskant points is of varying size and thickness when compared to the others. In some instances, the applied maskant may be partially abraded utilizing the grit blasting technique described previously for cleaning with an 80-120 mesh grit at 80-90 psi. to assist in providing an irregular maskant coating.
As shown in
Referring now to the illustration of
While a number of etchants could be utilized, the particular chemistry adopted for the described embodiment utilizes a standard 30% nitric acid-6% hydrofluoric acid combination which is commonly marketed and well known in the art. The etchant is applied at 110 degrees F. for approximately four minutes to achieve a desired 0.008-0.010 inch etch depth. This time period or the strength of the etchant solution may be adjusted upwardly or downwardly to achieve a heavier or lighter etching. The etching is halted in a water bath or spray. Post-etch the maskant material may be removed in a variety of ways, including mechanically or chemically. Depending on the size and number of coated objects, mechanical brushing or blasting of the maskant will peel it off. Additionally, the use of nitric acid is also contemplated to dissolve the maskant material.
Referring again to the lower illustration of
As shown in the lower illustration of
As can be seen in the lower illustration of
After performing the process described above in conjunction with
In addition to chemical etching as described above, the irregular exterior surface 231 (or 230) of connecting portion 223 can also be achieved using electrochemical etching. In one embodiment, electrochemical etching can be performed on the connecting portion 223 of rigid sections 201/203 made from a cobalt-chromium alloy base metal. While cobalt-chromium alloy is the described embodiment, a number of other alloys may be utilized in connection with electrochemical etching. Each of these different alloys may require a different maskant and electrochemical etching conditions. While no specific details are given in the specification regarding the use of these other metals and electrochemical etching conditions, it is considered to be well within the knowledge of a person of ordinary skill in the art to select the appropriate electrochemical etching conditions once a base alloy has been identified.
Once again referring now to
As described previously, the maskant is applied at a variety of points in a variety of stages. A typical electrochemical etching process involves applying a maskant material and curing the applied maskant material until the exterior surface 231 of connecting portion 223 is ready to be electrochemically etched. A tank may be used to submerge the tooling and connecting portion 223 under an electrolyte fluid. The electrolyte fluid fills the work gap between the tooling and the exterior surface 231 of connecting portion 223 The electrolyte fluid is pumped at controlled rate through a passageway in the tooling and out through an orifice into the work gap. The tooling is in electrical connection with the negative terminal of a direct current power supply and thus becomes the cathode of the electrochemical etching process. Connecting portion 223 is in electrical connection with the positive terminal of the same direct current power supply and thus becomes the anode of the electrochemical etching process.
The electrolyte fluid for electrochemically etching a cobalt-chromium alloy is preferably a solution containing the proportions of one pound each of NaCl and NaNO3 dissolved in one gallon of water. One skilled in the art of electrochemically etching metals will recognize and employ the appropriate electrolyte fluid to be used for the type of metal of a particular connecting portion 223. Control of the flow rate of the electrolyte fluid through the work gap is important because the electrolyte fluid must adequately remove both the heat and the reaction products of the electrochemical process. The optimum flow rate level is related to the amount of current employed. Higher ratios of flow rate to current give better removal of heat and reaction products. For the electrochemical etching a cobalt-chromium alloy, for example, the electrolyte fluid should flow through the work gap at a rate of about 0.15-0.5 gallons per minute per 100 amps and have a temperature of between about 100-130 degrees F. One skilled in the art of electrochemically etching metals will be able to determine the proper values of these parameters to use with a particular application.
The tooling may be made from any material suitable for use in electrochemical etching such as copper, nickel, or an alloy of tungsten-copper. The tooling should be configured so that the work gap between the tooling and the attachment surface is substantially uniform. This is accomplished by making the tooling substantially conformal to exterior surface 231. In one embodiment, the work gap is between approximately 0.020-0.250 inches, and in a more particular embodiment between approximately 0.060-0.120 inches. One skilled in the art of electrochemically etching metal will be able to determine the proper work gap to use for a particular application. A direct current voltage difference between the tooling and exterior surface 231 of between about 8V-24V and a specific amperage of at least about 50 amps per square inch of exposed portion 120 of exterior surface 231 are to be maintained during the electrochemical etching of a cobalt-chromium connecting portion 223. Preferably, the direct current voltage difference between the tooling and connecting portion 223 is between about 12-18V and the specific amperage is about 75-120 amps per square inch of exposed portion 120 of exterior surface 231. The values of these parameters for use with other materials are readily determinable by one skilled in the art of electrochemical etching metals The stated conditions will produce a metal removal rate of about 0.003 inch per minute when the connecting portion 223 material is a cobalt-chromium alloy. The time period and other parameters of the electrochemical etching process, particular the specific amperage, may be adjusted upwardly or downwardly to achieve a heavier or lighter etching. The electrochemical etching process is halted by removing the voltage difference between the tooling and connecting portion 223.
The maskant material on exterior surface 231 is removed after each electrochemical etching step. In the embodiment using a cobalt-chromium alloy exterior surface 231 and the Hysol ER1006 maskant material, the exterior surface 231 can be immersed in an aqueous solution of an alkaline cleaner to dissolve the maskant material, where the temperature of the alkaline cleaner solution is between about 80-145 degrees F. The immersion time can be about 5 to 10 minutes or until the maskant is removed. Water blasting is employed to remove any clinging maskant material which was softened by the alkaline cleaning solution.
In the embodiment shown in
Additional and/or alternative methods of forming an irregular surface on the exterior surface 231 of connecting portion 223 of first rigid section 201 and/or second rigid section 203 may be found in U.S. Pat. Nos. 5,258,098, 5,507,815, 5,922,029 and 6,193,762, each of which is hereby fully incorporated by reference herein.
As described earlier, embodiments of connection member 30 can comprise flexible section 202 molded around connecting portion 223 of first rigid section 201 and connecting portion 223 of second rigid section 202. In one embodiment, first rigid section 201 and/or second rigid section 203 will have had an appropriate exterior surface 231 formed (to include an irregular surface area, one or more features or both) on at least a portion of the connecting portion 223, then rigid sections 201 and 203 may be placed in a mold (not shown) that can be used in a molding process (such as an injection molding process) to create flexible section 202 molded about connecting portions 223 of first and second rigid section 201 and 203.
Once rigid sections 201 and 203 are positioned in the mold, material may be injection molded or otherwise molded around connecting portions 223 of rigid sections 201 and 203 to form flexible section 202 joined between the two rigid sections.
In some embodiments, flexible section 202 may be made of a material with properties that mimic or more naturally follow a natural human body response to applied loading. In many embodiments, flexible section 202 can be formed from a material has a modulus of elasticity that is less than the modulus of elasticity of rigid sections 201 and 203. Examples of suitable materials for flexible section 202 include polycarbonate urethane (PCU), Polyetheretherketone (PEEK), Polyetherketoneketone (PEKK), Ultra high molecular weight polyethylene (UHMWPE) or other similar materials. Other suitable materials are possible and would be known to those skilled in the art. Thus, as an example, if rigid sections 201 and 203 are manufactured from a material with a high modulus of elasticity (e.g., titanium), a material such as PEEK might be useful for flexible section 202, but if rigid sections 201 and 203 are manufactured from PEEK, it is preferable that flexible section 202 be manufactured from a material more flexible than PEEK.
The flexible material of flexible section 202 may be molded around connecting portion 223 so as to adhere to exterior surfaces 230 and 231 of connecting portion 223. Adherence may include, for example, material penetrating into apertures 226 or cannula 227, or enveloping boss 225. Adherence may also include material penetrating into portions of irregular exterior surface 231 formed on connecting portion 231 (or 230) of rigid section 201 or 203. In some embodiments, material of flexible section 202 joined to exterior surface 230 can inhibit the ingress of microorganisms, moisture, or other contaminants into the interior of stabilization rod 20. In one embodiment, the adherence of material to surface 230 may withstand an autoclave process. An advantage to forming connection member 30 to withstand an autoclave process may be the ability to use non-sterile packaging to package/ship connection member 30 without risk of contamination. In some embodiments, the adherence of the material of flexible section 202 to exterior surface 230 can also improve resistance to shear forces applied to connection member 30 at the junction between flexible section 202 and rigid sections 201 or 203. Embodiments of connection member 30 having rigid sections 201 and 203 with irregular surface patterns on surface 230 in contact with the molded material used to form flexible section 202 may also be able to withstand greater shear forces to provide greater stability once connection member 30 is implanted (e.g., coupled to the spine). Those skilled in the art may appreciate, after reading this disclosure, that by adjusting the thickness t of surface 230, the resistance to contamination or the shear strength may be improved.
It should be understood that while embodiments of connection member 30 shown in the drawings herein have rigid sections 201 that are identical to second rigid sections 203, embodiments of connection member 30 may include first rigid section 201 having a surface area or geometry that is different from that of second rigid section 203. It should further be understood that while in some embodiments, rigid sections 201 and 203 are positioned in a mold such that their longitudinal axes are aligned, thereby resulting in a generally straight implantable connection member 30, in alternative embodiments, rigid sections 201 and 203 may be positioned in a mold such that their longitudinal axes are at some desired angle. For example,
In alternative embodiment, connection member 30 can comprise more than three sections, with each additional section being either a rigid section 201/203 or a flexible section 202. Depending upon the pattern and/or length desired, the biocompatible material used to form additional rigid sections or flexible sections may be the same or different from one another. In one embodiment, all parts of connection member 30 are of equal or substantially similar size. In one embodiment, the length of each part may be the same or substantially the same. In one embodiment, the length of each part may vary. In one embodiment, one or both ends (e.g., rigid sections 201 and/or 203) of connection member 30 can extend to more than one level, making connection member 30 useful in a multi-level procedure.
One of the advantages of various embodiments dynamic connection member 30 is that flexible sections 202 provide stability in lateral bending, axial rotation and in shear while allowing some motion that mimics the motion of a healthy spine. As one skilled in the art can appreciate, the geometry of connection member 30 can vary according to the need and the operating level (e.g., thoracic, lumbar, etc.).
Stabilizing a spine may include determining a desired rigidity for a first portion of the spine and a second rigidity for a second portion of the spine, and utilizing connection members 30having rigid sections 201 and 203 and flexible sections 202 of selected lengths to preserve the desired rigidity for different vertebral levels. For example, spine 12 may have anchoring systems 18 implanted in three or more vertebrae 20, such as depicted in
Spinal stabilization system 10 may also include suitable transverse rods or cross-link devices that help protect the supported portion of spine 12 against torsional forces or movement. Some possible examples of suitable cross-link devices are shown in co-pending U.S. patent application Ser. No. 11/234,706, filed on Nov. 23, 2005 and naming Robert J. Jones and Charles R. Forton as inventors (the contents of this application are hereby fully incorporated by reference herein). Other known cross-link devices or transverse rods may also be employed to provide further support to spinal stabilization system 10.
Spinal stabilization systems incorporating embodiments of connection member 30 can provide a number of advantages over other stabilization systems. For example, when properly installed, spinal stabilization system 10 may minimize torsional and shear stresses that tend to delaminate an intervertebral disc at a first vertebral level and may further protect an adjacent level from stresses, which may eliminate or reduce adjacent level disc degeneration. Spinal stabilization system 10 may also be able to provide superior pain relief by restricting undesirable spine motion by providing stability in lateral bending, torsion and shear, while simultaneously allowing movement in flexion-extension. Embodiments of spinal stabilization system 10 may be used in minimally invasive surgery (MIS) procedures as well as non-MIS procedures. It is believed that the ability to implant spinal stabilization system 10 using MIS procedures can provide additional advantages. MIS procedures seek to reduce cutting, bleeding, and tissue damage or disturbance associated with implanting a spinal implant in a patient's body. Exemplary procedures may use a percutaneous technique for implanting longitudinal rods and coupling elements. Examples of MIS procedures and related apparatus are provided in U.S. patent application Ser. No. 10/698,049, filed Oct. 30, 2003, U.S. patent application Ser. No. 10/698,010, filed Oct. 30, 2003, and U.S. patent application Ser. No. 10/697,793, filed Oct. 30, 2003, each of which is fully incorporated herein by reference.
In the foregoing specification, specific embodiments have been described with reference to the accompanying drawings. However, as one skilled in the art can appreciate, embodiments of the connection rod disclosed herein can be modified or otherwise implemented in many ways without departing from the spirit and scope of the disclosure. Accordingly, this description is to be construed as illustrative only and is for the purpose of teaching those skilled in the art the manner of making and using embodiments of a connection member having a flexible section between two rigid sections. It is to be understood that the embodiments shown and described herein are to be taken as exemplary. Equivalent elements or materials may be substituted for those illustrated and described herein. Moreover, certain features of the disclosure may be utilized independently of the use of other features, all as would be apparent to one skilled in the art after having the benefit of this description of the disclosure.