Vertebral body placement and method for spanning a space formed upon removal of a vertebral body

Abstract
A vertebral body replacement includes first and second end plates, and a compliant connector section between the end plates having one or more helical cuts to provide limited compliance between the end plates. The compliant connector section can be provided in a separate spacer that fits between the end plates or directly in one or more of the end plates. The adjoining end plate surfaces, and/or adjoining surfaces of the spacer, include a rotational interlock to inhibit rotational motion between the surfaces and allow a modular stacking assembly of the vertebral body replacement to accommodate a wide range of patients.
Description
CROSS-REFERENCES TO RELATED APPLICATIONS

This application claims priority under 35 U.S.C. §119 to U.S. Provisional Application No. 60/981,665 filed Oct. 22, 2007, entitled “Method and Spacer Device Spanning Space Formed Upon Removal of an Intervertebral Disc,” the full disclosure of which is incorporated herein by reference.


BACKGROUND OF THE INVENTION

The present invention relates to medical devices and methods. More specifically, the invention relates to vertebral body replacements and methods of spanning a space formed upon removal of an intervertebral disc.


Back pain takes an enormous toll on the health and productivity of people around the world. According to the American Academy of Orthopedic Surgeons, approximately 80 percent of Americans will experience back pain at some time in their life. In the year 2000, approximately 26 million visits were made to physicians' offices due to back problems in the United States. On any one day, it is estimated that 5% of the working population in America is disabled by back pain.


One common cause of back pain is injury, degeneration and/or dysfunction of one or more intervertebral discs. Intervertebral discs are the soft tissue structures located between each of the thirty-three vertebral bones that make up the vertebral (spinal) column. Essentially, the discs allow the vertebrae to move relative to one another. The vertebral column and discs are vital anatomical structures, in that they form a central axis that supports the head and torso, allow for movement of the back, and protect the spinal cord, which passes through the vertebrae in proximity to the discs.


Another form of spinal injury involves injury or deformity of the vertebra themselves. When one or more vertebrae is fracture or deformed by tumor or other causes and results in pain and discomfort, surgery is often required. Traditionally, surgical procedures for vertebral replacement have involved removal of the vertebra and fusion of the two vertebrae above and below the missing vertebra. It is necessary to replace the removed vertebra to maintain spacing of adjacent vertebrae. Oftentimes, pins, rods, screws, cages and/or the like are inserted between the vertebrae to act as support structures to hold the vertebrae and graft material in place while they permanently fuse together. These vertebral body replacement procedures generally focus on rigidly fusing the adjacent vertebrae and preventing motion.


However, it would be desirable to achieve immobilization of the vertebrae adjacent a removed vertebral body and maintain spacing between the adjacent vertebrae without the complete rigidity of traditional interbody fusion.


Another problem associated with the typical vertebral body replacement procedure is the subsidence of the cage into the vertebral body. The typical vertebral body replacement cage is formed with a large percentage of open space to allow the bone to grow through and form the bridging bone which immobilizes the vertebrae. However, the large amount of open space means that the load on each segment of the cage is significantly higher than if the cage surface area was larger. This results in the cage subsiding or sinking into the bone over time and allows the space between the vertebrae to collapse.


Therefore, a need exists for improved vertebral body replacement and method for spanning a space and maintaining spacing between two vertebrae after removal of an intervertebral body. Such improved method and intervertebral body replacement would avoid the need for growth of bridging bone between the remaining vertebrae.


BRIEF SUMMARY OF THE INVENTION

Embodiments of the present invention provide a vertebral body replacement with compliance or shock absorption and methods of spanning a space formed upon removal of vertebral body.


In accordance with one of numerous aspects of the present invention, a vertebral body replacement for replacing at least one vertebral body between remaining upper and lower vertebral bodies, the vertebral body replacement comprises a first end plate having an upper surface configured to engage against a surface of the upper remaining vertebral body, and a lower surface opposite the upper surface spanning the first end plate, a second end plate having a lower surface configured to engage against a surface of the lower remaining vertebral body, and a compliant connector section between the first end plate lower surface and the second end plate lower surface, the compliant connector section comprising at least one helical cut configured and arranged to permit limited motion between the first end plate and the second end plate.


In accordance with another aspect of the invention, a method of replacing at least one vertebral body comprises removing said at least one vertebral body between two remaining vertebral bodies, placing a vertebral body replacement between said two remaining vertebral bodies, the vertebral body replacement comprising first and second end plates and a compliant connector section between the first and second end plates, the compliant connector section having at least one helical cut and configured and arranged to limit motion to less than 10 degrees between said remaining vertebral bodies, and maintaining the space between the two remaining vertebral bodies with the vertebral body replacement.





BRIEF DESCRIPTION OF THE DRAWINGS


FIG. 1 is a perspective view of a vertebral body replacement according to one embodiment of the present invention;



FIG. 1A is an exploded, perspective view of the vertebral body replacement of FIG. 1;



FIG. 2 is a perspective view of a vertebral body replacement according to a second exemplary embodiment of the present invention; and



FIG. 3 is a perspective view of a vertebral body replacement according to a third exemplary embodiment of the present invention.





DETAILED DESCRIPTION OF THE INVENTION

Various embodiments of the present invention generally provide for a vertebral body replacement having upper and lower plates or surfaces connected by a central connector portion which provides some limited amount of axial compliance and/or rotational motion between the upper and lower plates or surfaces. The compliant vertebral body replacement according to the present invention can maintain disc height and prevent subsidence with a large surface area while improving outcomes by allowing some limited motion and providing improved fixation. The compliance of the vertebral body replacement also functions to reduce loading on the interface between the bone and vertebral body replacement.


One example of a vertebral body replacement 10 for replacement of a vertebral body and maintaining disc height between two adjacent vertebral discs is shown in FIG. 1. The body 10 includes at least one end plate 20 having a vertebral body contacting surface 24, a second end plate or body end 30 opposite the end plate 20, and a compliant connector or connector section 32 interposed between, or interconnecting, the two ends 20, 30. As will be described below, some limited rotational and axial motion may be provided between the two plates or sections 20, 30 to reduce loading on the interface between the adjacent vertebral bodies and the body 10. According to an exemplary device embodying principles of the present invention, the compliance of the connector 32, as well as some small amount of translation and rotation, is provided by lateral cuts or slots 70 extending into the connector 32. The body 10 when implanted between two vertebrae maintains a desirable space between the two adjacent vertebrae similar to that provided by a natural vertebra.


Although the body 10 has been shown as generally oblong in cross section, other shapes may be used, including circular, oval, elliptical, or rectangular. Although the connector section 32 has been illustrated in FIG. 1 as integral with the end section 30, according to other embodiments, the connector can include one or more separate compliant connectors or spacers in other configurations and at other locations. By way of example, a compliant connector may be the same or substantially the same diameter, size, and shape as the plates, multiple connectors can be arranged in a rectangular pattern, or a hollow cylindrical connector can be used. Further optionally, while the surfaces 24 are illustrated being perpendicular to the vertical axis of the body 10, one or both of the surfaces 24 can be somewhat wedge-shaped, formed with one or two lordosis angles, as well known to those of ordinary skill in the art. The modular design of the upper plate 20 and the lower plate section 30 allows the creation of a complete bodies 10 of different sizes to correspond to the particular space for each patient.


The upper plate 20 and the lower plate or plate section 30, and connector 32, may be constructed from any suitable metal, alloy or combination of metals or alloys, such as but not limited to cobalt chrome alloys, titanium (such as grade 5 titanium), titanium based alloys, tantalum, nickel titanium alloys, stainless steel, and/or the like. They may also be formed of ceramics, biologically compatible polymers including PEEK, UHMWPE (ultra high molecular weight polyethylene) or fiber reinforced polymers. However, when polymer is used for the body 10, the contacting surfaces 24 may be coated or otherwise covered with metal for fixation. The upper plate 20 and the lower plate or plate section 30, and connector 32, may be formed of a one piece construction or may be formed of more than one piece, such as different materials coupled together. When the body 10 is formed of multiple materials, these materials are fixed together to form a unitary one piece spacer without separately moving parts.


Different materials may be used for different parts of the body 10 to optimize imaging characteristics. For example, the upper plate 20 and the lower plate or plate section 30 may be formed of titanium, while the connector 32 is formed of cobalt chromium alloy for improved imaging of the plates. Cobalt chrome molybdenum alloys, when used for the plates 20, 30 may be treated with aluminum oxide blasting followed by a titanium plasma spray to improve bone integration. Other materials and coatings can also be used such as titanium coated with titanium nitride, aluminum oxide blasting, HA (hydroxylapatite) coating, micro HA coating, and/or bone integration promoting coatings. Any other suitable metals or combinations of metals may be used as well as ceramic or polymer materials, and combinations thereof. Any suitable technique may be used to couple materials together, such as snap fitting, slip fitting, lamination, interference fitting, use of adhesives, welding and/or the like.


In some embodiments, the outer surface 24 is planar. Oftentimes, the outer surface 24 will include one or more surface features and/or materials to enhance attachment of the body 10 to vertebral bone. For example, as shown in FIG. 1, the outer surface 24 may be machined to have serrations 40 or other surface features for promoting adhesion of the plates 20, 30 to a vertebra. In the embodiment shown, the serrations 40 are pyramid shaped serrations extending in mutually orthogonal directions, but other geometries such as teeth, grooves, ridges, pins, barbs or the like would also be useful. When the bone integration structures are ridges, teeth, barbs or similar structures, they may be angled to ease insertion and prevent migration. These bone integration structures can be used to precisely cut the bone during implantation to cause bleeding bone and encourage bone integration. Additionally, the outer surface 24 may be provided with a rough microfinish formed by blasting with aluminum oxide microparticles or the like to improve bone integration. In some embodiments, the outer surface may also be titanium plasma sprayed or HA coated to further enhance attachment of the outer surface 24 to vertebral bone.


The outer surfaces 24 may also carry one or more upstanding fins 50, 52 which also extend laterally in an anterior-posterior direction. The fins 50, 52 are configured to be placed in slots in the vertebral bodies. Preferably, the fins 50, 52 each have a height greater than a width and have a lateral length greater than the height. In one embodiment, the fins 50, 52 are pierced by transverse holes 54 for bone ingrowth. The transverse holes 54 may be formed in any shape and may extend partially or all the way through the fins 50, 52. In alternative embodiments, the fins 50, 52 may be rotated away from the anterior-posterior axis, such as in a lateral-lateral orientation, a posterolateral-anterolateral orientation, or the like.


The fins 50, 52 provide improved attachment to the bone and prevent rotation of the plates 20, 30 in the bone. In some embodiments, the fins 50, 52 may extend from the surface 24 at an angle other than 90°. For example, on one or more of the plates 20, 22 where multiple fins 52 are attached to the surface 24, the fins may be canted away from one another with the bases slightly closer together than their edges at an angle such as about 80-88 degrees. The fins 50, 52 may have any other suitable configuration including various numbers angles and curvatures, in various embodiments. In some embodiments, the fins 50, 52 may be omitted altogether. The embodiment of FIG. 1 illustrates a combination of one plate with a single fin 50 and another plate with a double fin 52. This arrangement is useful for double level disc replacements and utilizes offset slots in the vertebral body to prevent the rare occurrence of vertebral body splitting by avoiding cuts to the vertebral body in the same plane for multi-level implants. The combination of the single fin 50 and double fin 52 can also assist the surgeon in placement of the spacer in the correct orientation.


The body 10 has been shown with the fins 50, 52 as the primary fixation feature; however, the fins may also be augmented or replaced with one or more screws extending through the plates and into the bone. For example in the body 10 of FIG. 1, the upper fin 50 may be augmented or replaced with one or more screws (not illustrated) while the two lower fins 52 remain. The plates 20, 30 can be provided with one or a series of holes 60 to allow screws to be inserted at different locations at the option of the surgeon. However, the holes 60 should not be of such size or number that the coverage of the plate 20, 30 is decreased to such an extent that subsidence occurs. Alternately, the screws can pass laterally through one or more of the holes in the fins. When one or more screws are provided, they may incorporate a locking feature to prevent the screws from backing out. The screws may also be provided with a bone integration coating.


Some limited holes may also be provided in the plate to allow bone ingrowth. However, if the outer surfaces 24 have holes therein, the holes advantageously cover less than 40 percent of the outer surface 24 which contacts the bone to prevent subsidence of the plates into the vertebral bodies. Preferably the holes will cover less than 25 percent, and more preferably less than 10 percent of the outer bone contacting surfaces. At the option of the surgeon, when the small holes are present in the plates 20, 30, bone graft can be placed in the holes to allow bone to grow through the plates. The embodiments illustrated in FIGS. 1-3 also illustrate the optional inclusion of countersunk screw holes 60 extending between a lateral surface of the plates 20, 30 and the end surfaces 24, in which bone screws may optionally be inserted to further stabilize the body 10. The holes 60 can alternatively extend vertically through the end plates, or the end plates can include combinations of vertical and angled holes.


The vertebral body replacement 10 shown herein is configured for placement in the vertebral column from an anterior approach. It should be understood that other approaches can be used, and the particular shape of the vertebral body replacement would be modified depending on the approach. For example, for a lateral approach, the vertebral body replacement may be formed in a more elongated, kidney bean, or banana shape with a transversely oriented fin.


As shown in FIG. 1, the vertebral body replacement 10 is provided with shock absorption or some other limited motion between the two plates 20, 30 by providing a compliant connector 32. The limited motion provided by the compliant connector 32 is designed to reduce forces on the interface between the outer surfaces 24 and the bone to improve long term fixation of the spacer. The compliance of the connector 32 allows motion between the vertebral bodies to be accommodated by the compliance in the body 10 rather than causing one or both of the vertebral bodies to pull away from the plates 20, 30. The compliant connector 32 provides limited relative motion between the plates, which may include compliance in a vertical direction of up to about 6 mm, rotation in an anterior/posterior direction, lateral direction, or axial rotation of less than about 10 degrees, and/or translation of up to about 1 mm.


In the vertebral body replacement 10 of FIG. 1, the compliance, as well as some small amount of translation and rotation, is provided by the cuts or slots 70 extending into the connector 32. In the embodiment of FIG. 1, the slots 70 are spiral slots, however, other shaped slots may also be used. The compliant connector 32 is advantageously formed as a unitary member with at least one lateral cut or slot 70 positioned between the upper and lower plates 20, 30, permitting the plates to move resiliently toward and away from each other. The replacement 10 can also be formed as multiple parts where different properties are desired from the different parts, such as different radiopacities, different strengths, or different flexibility properties and for flexibility in creating the size and configuration of spacer suited to the patient. The lateral cuts 70 in the connector 32 allow the connector to function as a compliant member without affecting the function of the upper and lower plates of the body 10.



FIG. 2 illustrates an alternative embodiment of a body 10 having multiple parts including end plates 20, 30 and spacers 90. The spacers 90 include lateral cuts 70 in place of the spiral cuts of FIG. 1. The material remaining after the cuts 70 are made is called a column. A shallow cut, that is, one that extends laterally into the connector a relatively small distance, and a large column provides a stiffer spacer, while a deeper cut and smaller column provides a more compliant spacer. In the embodiment shown in FIG. 2, the cuts 70 are at least 60% of the way through the spacer width or diameter, and preferably at least 75% of the way through the connector width.


Optionally, a variable stiffness shock absorbing connector 32 (FIG. 1) or spacer 90 (FIG. 2) can be constructed with lateral cuts 70 with tapering widths. For cuts with such tapering widths, the cut 70 is smallest where the cut terminates adjacent the column and is largest at the edge of the connector 32 furthest from the column. In this version, each of the lateral cuts 70 causes the connector 32 to act as a non linear spring providing progressively stiffer behavior upon larger compression. This is due to the fact that progressively more material on the sides of the cuts 70 is in contact as the connector 32 or spacer 90 is compressed. The non-linear spring can be incorporated in any of the other embodiments described herein to provide a softer stop to the compliant action of the core. The tapered width cuts 70 can provide the additional benefit of providing a flushing action during operation that moves any accumulated material out of the cuts.


The cuts 70 also advantageously include a stress relief 74 at the end of the cuts which increases the fatigue life of the device by reducing the stress concentration at the ends of the slots.


In the exemplary embodiments illustrated herein, a shock absorbing connector 32 includes either one or more planar cuts 70 (FIG. 2), or alternatively one or more spiral or helical cuts 70 (FIG. 1) to form one or more continuous spring coil elements 72 which provide compliance to the connector. Although the spiral cut connector 32 is illustrated in FIG. 1 with two spiral cuts, only one, or three or more spiral cuts may also be employed. For example, two or more spiral cuts 70 arranged in opposite directions can be formed in the connector 32, as illustrated in FIG. 1. Furthermore, when more than one spiral cut 70 is provided, the cuts can optionally be nested one inside the other (not illustrated), as in the manner of a multi-start thread, and/or can include combinations of both nested and adjacent cuts (such as those illustrated in FIGS. 1-2). The compression of a spiral cut connector 70 can result in some small amount of relative rotation between the upper and lower surfaces 20, 30. In cases where it is desirable to eliminate this rotation, a connector 32 having multiple spiral cuts in opposite directions can be used. For example, a connector 32 can be formed with a first spiral cut 70 at a top of the connector in a first direction and a second spiral cut 70 at a bottom of the core in an opposite second direction. The first and second spiral cuts can offset rotation of each other resulting in a non rotating compliant connector. The double spiral embodiment of the connector is also more stable in shear than the single coil. Furthermore, coils 74 provide significantly more surface area between the adjoining surfaces of the cuts 70 than do planar cuts, which can be advantageous to allow limited rotational motion. The spiral cuts 70 can be made parallel to the end surfaces of the body 10 or can be angled, as in a cone shape. When the spiral cuts 70 are angled to form a cone shaped spring the cone shaped surfaces can limit the translational movement of the spring.


In each of the shock absorbing connectors described herein, the interconnected sections within the connector and the plate(s) are designed for minimal or no motion between contacting parts to prevent particulate generation. However, since the plates and connectors are made entirely of hard materials such as metals, some minimal rubbing contact may be accommodated. In the exemplary embodiments illustrated in figures herein, a rotational interlock 80 is provided between the lower surface of the end plate 20 and the adjoining upper surface of the connector section 32 of the end plate 30. With reference to FIG. 2, the exemplary interlock 80 includes complementary portions 82, 84, formed on the adjoining faces of the end plate 20 and the connector section 32, in the exemplary body 10, taking the shape of simple raised portions or ribs 84 which mate with correspondingly sized and shaped recesses 82. The rotational interlock 80 is not limited to the particular shapes or orientations illustrated in the drawing figures, and can take any shape or orientation which resists, and advantageously prevents, the plate 20 and the connector section 32 from rotating relative to each other. The rotational interlock 80 on the top and bottom surface of a spacer 90 can be different to allow the complete body 10 to be assembled only in a particular desired configuration.


Further optionally, as illustrated in FIG. 1A, the body 10 can include one or more blind cavities 86 extending vertically through the connector section 32, which provides the interior side of the spiral cut 70. The blind cavities 86 can also vary in cross sectional size and shape to tailor the rigidity of the connector section 32 in different directions. More specifically, the cavity or cavities 86, only one of which is illustrated in FIG. 1A, when left hollow, provides a less rigid connector 32. To increase the rigidity of the connector section 32, other material can be used to partially or completely fill the cavity 86, such as pins or rods (not illustrated) inserted in the cavity.


When implanted between vertebrae, the shock absorbing connector 32 can resiliently absorb shocks transmitted vertically between upper and lower vertebrae of the patient's spinal column. This shock absorption is related to the material properties, design, and dimensions of the connector. In general, an increased number and width of the cuts 70 will increase absorption of shocks, with more elastic, or springy compression between the vertebrae.


Preferably the connector 32 is made of metal such as titanium, cobalt chromium alloy, stainless steel, tantalum, nickel titanium or a combination thereof. These materials also can be designed to provide a device which is deformable in the elastic region of the stress/strain curve and will not plastically deform during compression.


In the embodiments illustrated herein, the number, pitch, lead, lead angle, handedness, and total vertical length of each of the spiral cuts or slots 70, as well as the combination of multiple cuts if provided, can be varied to change the amount of compliance of the connector 32. When a load is applied to the upper and lower plates 20, 30, the connector 32 will compress with each of the cuts 70 closing and the total amount of compression possible depending on the number, arrangement, and height of the cuts. The cuts 70 form spiral coils 74 between the ends of the cut, which function like springs to allow the connector 32 to be compressed. The cuts 70 may be modified to be non-uniform to provide preferential deflection in one or more bending directions. Preferential deflection is useful to provide increased anterior-posterior compliance and less lateral compliance, or the other way around.


According to one embodiment of the invention, the cuts 70 in the shock absorbing connector 32 according to any of the embodiments described herein may be manufactured by wire EDM (electrical discharge machining), molding, laser cutting, or the like. A number of cuts 70 can vary from 1 to about 50, preferably about 6 to about 20, for a vertebral body replacement. A width of the lateral cuts 70 in the direction of the height of the body 10 is about 0.01 mm to about 2 mm, preferably about 0.05 to about 1 mm.


In one embodiment of the present invention, for a cervical application, the maximum deformation of the shock absorbing body is about 0.5 to about 4 mm, and is preferably about 1 to about 2 mm. For a lumbar application, the maximum deformation of the shock absorbing body is about 1 to about 6 mm, and is preferably about 1 to about 3 mm.


Although motion between the plates 20, 30 of the body 10 has been described herein as provided by cuts 70, it should be understood that this motion can be provided in a number of other known manners, such as use of resilient materials, or movable joints as long as the motion is limited to the small amount of motion allowable in a patient requiring a fusion procedure including compliance or vertical motion between the plates of up to about 6 mm, rotation between the plates of less than 10 degrees, and translation between the plates of up to about 1 mm.


The body 10 can be provided in different sizes, with different plate sizes, angles between plates, lordosis angles, and heights for different patients or applications. In addition, the shock absorbing connector section 32 can be provided in different compliances for different patients. In addition, the compliance and/or height of the body 10 can be adjustable, such as by rotating an adjustment screw before or after implantation, and/or bonding portions of one or more of the portions of a coil 74. The body 10 preferably is sized to provide substantial coverage of the vertebral surfaces. For example, in an anterior procedure, the plates 20, 30 are preferably sized to cover at least 50 percent of the vertebral surface. In posterior or lateral procedures, the coverage of the vertebral surface may be somewhat smaller due to the small size of the access area, i.e., the posterior or lateral spacers may cover about 40 percent or more of the vertebral surface with a one or two part spacer.


Turning now to FIG. 2, a second exemplary embodiment of a body 10, adhering to principles of the present invention, is illustrated. In contrast to the embodiment illustrated in FIGS. 1 and 1A, the body 10 illustrated in FIG. 2 includes one or more separate compliant connector spacers 90 positioned between plates 20, 30, rather than a connector section 32 of a plate 30. Each of the spacers 90 includes one or more cuts 70, which can be either planar cuts or forming one or more coils, as described above with reference to the embodiment of FIGS. 1 and 1A. The adjoining surfaces of the plates 20, 30 and the spacers 90 are also provided with rotational interlocks 80, as described herein; while FIG. 2 suggests that the interlocks 80 are the same, differently configured interlocks can alternatively be provided for different non-adjoining surfaces, for example to prevent the spacers 90 from being assembled in a way other than that designed for a body 10 configured for the particular patient. By way of non-limiting example, a first rotational interlock, formed of rectangular ribs and recesses on adjoining surfaces of the end plates and/or the spacers, as illustrated in FIG. 1A, can be provided on the adjoining surfaces of the plate 20 and the adjacent first spacer 90; a second rotational interlock, formed of vertically oriented cylindrical pins, can be provided on the opposite face of the first spacer 90 and the adjoining surface of the adjacent spacer or plate 30. Because the two interlocks 80 are incompatible and do not mate, there is only a single configuration of the pieces that will permit them to be assembled into a body 10.



FIG. 3 illustrates a third exemplary embodiment of a body 10, adhering to principles of the present invention. In addition to the features previously described with reference to FIGS. 1-2, the embodiment illustrated in FIG. 3 includes a vertical adjustment mechanism 100 for fine tuning of the vertical size of the body 10, either prior to or after implantation of body 10 into a patient. While numerous configurations of the adjustment mechanism 100 can be provided, one exemplary embodiment includes a threaded post or tube 102 extending from either an upper surface 106 of the end plate 30 or a lower surface 104 of the section 32, which mates with a correspondingly configured and threaded hole or post in the other of the end plate 30 and section 32. Rotation of the post 102 causes the two portions of the body 10 to move toward or away from each other, and thus decreases or increases the vertical size of the body 10, respectively. According to one version of the adjustable height vertebral body replacement an adjustment mechanism with oppositely threaded ends is inserted in the upper and lower parts 104, 106 and is adjustable after positioning in the patient.


According to one exemplary method adhering to principles of the present invention, a patient in need of a vertebral body replacement is prepped and surgical access is made to the particular vertebral body to be removed. Access to the surgical site is generally made anteriorly through the abdominal cavity for a lumbar procedure. One or more target vertebral body or bodies is removed in one of numerous manners known to those of ordinary skill in the art, between upper and lower remaining vertebral bodies in the patient's spine, and a vertebral body replacement 10, embodying principles of the present invention, is selected based on the measurement of the spacing for proper spinal alignment. The vertebral body replacement 10 is assembled and implanted in the space created by removal of the original vertebral body or bodies. Optionally, one or more spacers 90 are assembled into the body 10, prior to installation of the body 10 into the patient, and/or the vertical length of the body 10 is adjusted to better fit in the space. Further optionally, when the body 10 includes one or more cavities 86, additional material is inserted into the cavity, prior to implantation of the body, to tailor the rigidity of the body 10, or for other purposes.


While the exemplary embodiments have been described in some detail, by way of example and for clarity of understanding, those of skill in the art will recognize that a variety of modifications, adaptations, and changes may be employed. Hence, the scope of the present invention should be limited solely by the appended claims.

Claims
  • 1. A vertebral body replacement for replacing at least one vertebral body between remaining upper and lower vertebral bodies, the vertebral body replacement comprising: a first end plate having an upper surface configured to engage against a surface of the upper remaining vertebral body, and a lower surface opposite the upper surface spanning the first end plate;a second end plate having a lower surface configured to engage against a surface of the lower remaining vertebral body;a compliant connector section between the first end plate lower surface and the second end plate lower surface, the compliant connector section comprising a plurality of separate stackable spacers each having at least one helical cut configured and arranged to permit limited rotation between the first end plate and the second end plate in an anterior/posterior direction and a lateral direction; anda rotational interlock on the first end plate lower surface and an upper surface of at least one of the spacers, the rotational interlock being configured and arranged to inhibit rotational motion between the first end plate lower surface and the at least one spacer upper surface,wherein the rotational interlock comprises a first raised elongate portion extending in the anterior/posterior direction or the lateral direction on one of the first end plate lower surface or the at least one spacer upper surface and a first complementary elongate recess in the opposite surface.
  • 2. The vertebral body replacement of claim 1, wherein the second end plate includes an upper surface opposite the second end plate lower surface and spanning the second end plate, the compliant connector section located between the second end plate lower and upper surfaces.
  • 3. The vertebral body replacement of claim 2, wherein said rotational interlock is a first rotational interlock, and further comprising a second rotational interlock on the first end plate lower surface and the second end plate upper surface, the second rotational interlock configured and arranged to at least inhibit rotational motion between the first end plate lower surface and the second end plate upper surface.
  • 4. The vertebral body replacement of claim 1, wherein the compliant connector section is configured and arranged to limit motion to less than 10 degrees between said remaining vertebral bodies.
  • 5. The vertebral body replacement of claim 1, wherein the at least one helical cut in each of the separate stackable spacers are oppositely oriented.
  • 6. The vertebral body replacement of claim 1, wherein said rotational interlock is a first rotational interlock, wherein the at least one spacer has a lower surface spanning the at least one spacer, wherein the second end plate has an upper surface spanning the second end plate, and further comprising: a second rotational interlock on the second end plate upper surface and the at least one spacer lower surface, the second rotational interlock configured and arranged to at least inhibit rotational motion between the second end plate upper surface and the at least one spacer lower surface,wherein the second rotational interlock comprises a second raised elongate portion extending in the anterior/posterior direction or the lateral direction on one of the second end plate upper surface or the at least one spacer lower surface and a second complementary elongate recess in the opposite surface.
  • 7. The vertebral body replacement of claim 6, wherein the first and second rotational interlocks are different.
  • 8. The vertebral body replacement of claim 1, further comprising: an adjustment mechanism between the first and second end plates, the adjustment mechanism configured and arranged to selectively move the first and second end plates towards and away from each other.
  • 9. The vertebral body replacement of claim 1, further comprising at least one bone ingrowth hole in at least one of the first and second end plates.
  • 10. The vertebral body replacement of claim 1, wherein each of the first and second end plates comprise a lateral surface, and wherein the at least one bone ingrowth hole extends between said lateral surface and said surface configured to engage against a surface of a remaining vertebral body.
  • 11. The vertebral body replacement of claim 1, wherein the vertebral body replacement is sized and shaped to replace one or more entire vertebral bodies of the human spine.
  • 12. A vertebral body replacement for replacing at least one vertebral body between remaining upper and lower vertebral bodies, the vertebral body replacement comprising: a first end plate having an upper surface configured to engage against a surface of the upper remaining vertebral body, and a lower surface opposite the upper surface spanning the first end plate;a second end plate having a lower surface configured to engage against a surface of the lower remaining vertebral body;a compliant connector section between the first end plate lower surface and the second end plate lower surface, the compliant connector section comprising a plurality of separate stackable spacers each having at least one helical cut configured and arranged to form a continuous spring coil element; anda rotational interlock on the first end plate lower surface and an upper surface of at least one of the spacers, the rotational interlock being configured and arranged to inhibit rotational motion between the first end plate lower surface and the at least one spacer upper surface,wherein the rotational interlock comprises a raised elongate portion extending in the anterior/posterior direction or the lateral direction on one of the first end plate lower surface or the at least one spacer upper surface and a complementary elongate recess in the opposite surface.
  • 13. The vertebral body replacement of claim 12, wherein the vertebral body replacement is sized and shaped to replace one or more entire vertebral bodies of the human spine.
  • 14. A vertebral body replacement for replacing at least one vertebral body between remaining upper and lower vertebral bodies, the vertebral body replacement comprising: a first end plate having an upper surface configured to engage against a surface of the upper remaining vertebral body, and a lower surface opposite the upper surface spanning the first end plate;a second end plate having a lower surface configured to engage against a surface of the lower remaining vertebral body and an upper surface;a compliant connector section between the first end plate lower surface and the second end plate lower surface, the compliant connector section comprising a plurality of separate stackable spacers each having at least one helical cut configured and arranged to form a continuous spring coil element; anda rotational interlock on the second end plate upper surface and a lower surface of at least one of the spacers, the rotational interlock being configured and arranged to inhibit rotational motion between the second end plate upper surface and the at least one spacer lower surface,wherein the rotational interlock comprises a raised elongate portion extending in the anterior/posterior direction or the lateral direction on one of the second end plate upper surface or the at least one spacer lower surface and a complementary elongate recess in the opposite surface.
  • 15. The vertebral body replacement of claim 14, wherein the vertebral body replacement is sized and shaped to replace one or more entire vertebral bodies of the human spine.
  • 16. A vertebral body replacement for replacing at least one vertebral body between remaining upper and lower vertebral bodies, the vertebral body replacement comprising: a first end plate having an upper surface configured to engage against a surface of the upper remaining vertebral body, and a lower surface opposite the upper surface spanning the first end plate;a second end plate having a lower surface configured to engage against a surface of the lower remaining vertebral body and an upper surface opposite the lower surface and spanning the second end plate;a compliant connector section between the first end plate lower surface and the second end plate lower surface, the compliant connector section comprising a plurality of separate stackable spacers each having at least one helical cut configured and arranged to permit limited rotation between the first end plate and the second end plate in an anterior/posterior direction and a lateral direction; anda rotational interlock on the second end plate upper surface and a lower surface of at least one of the spacers, the rotational interlock being configured and arranged to inhibit rotational motion between the second end plate upper surface and the at least one spacer lower surface,wherein the rotational interlock comprises a raised elongate portion extending in the anterior/posterior direction or the lateral direction on one of the second end plate upper surface or the at least one spacer lower surface and a complementary elongate recess in the opposite surface.
  • 17. The vertebral body replacement of claim 16, wherein the compliant connector section is located between the second end plate lower and upper surfaces.
  • 18. The vertebral body replacement of claim 16, wherein the compliant connector section is configured and arranged to limit motion to less than 10 degrees between said remaining vertebral bodies.
  • 19. The vertebral body replacement of claim 16, wherein the at least one helical cut in each of the separate stackable spacers are oppositely oriented.
  • 20. The vertebral body replacement of claim 16, wherein said rotational interlock is a first rotational interlock, and further comprising a second rotational interlock on the first end plate lower surface and the second end plate upper surface, the second rotational interlock configured and arranged to at least inhibit rotational motion between the first end plate lower surface and the second end plate upper surface.
  • 21. The vertebral body replacement of claim 16, further comprising: an adjustment mechanism between the first and second end plates, the adjustment mechanism configured and arranged to selectively move the first and second end plates towards and away from each other.
  • 22. The vertebral body replacement of claim 16, further comprising at least one bone ingrowth hole in at least one of the first and second end plates.
  • 23. The vertebral body replacement of claim 16, wherein each of the first and second end plates comprise a lateral surface, and wherein the at least one bone ingrowth hole extends between said lateral surface and said surface configured to engage against a surface of a remaining vertebral body.
  • 24. The vertebral body replacement of claim 16, wherein the vertebral body replacement is sized and shaped to replace one or more entire vertebral bodies of the human spine.
  • 25. A vertebral body replacement for replacing at least one vertebral body between remaining upper and lower vertebral bodies, the vertebral body replacement comprising: a first end plate having an upper surface configured to engage against a surface of the upper remaining vertebral body and at least one elongated fin on the upper surface configured to enter a slot cut in the upper remaining vertebral body;a second end plate having a lower surface configured to engage against a surface of the lower remaining vertebral body and at least one elongated fin on the lower surface configured to enter a slot cut in the lower remaining vertebral body;a compliant connector section between the first end plate and the second end plate, the compliant connector section comprising a plurality of separate stackable spacers each having at least one helical cut configured and arranged to permit limited rotation between the first end plate and the second end plate in an anterior/posterior direction and a lateral direction, wherein the compliant connector section is configured and arranged to limit motion to less than 10 degrees between said remaining vertebrae.
  • 26. The vertebral body replacement of claim 25, wherein the upper and lower surfaces have less than 10 percent comprising holes.
  • 27. The vertebral body replacement of claim 25, further comprising one or more holes in the first and second end plates configured to receive screws extending through the plates and into the bone.
US Referenced Citations (452)
Number Name Date Kind
3867728 Stubstad et al. Feb 1975 A
4309777 Patil Jan 1982 A
4531917 Linkow et al. Jul 1985 A
4566466 Ripple et al. Jan 1986 A
4619660 Christiansen et al. Oct 1986 A
4673407 Martin Jun 1987 A
4759766 Buttner-Janz et al. Jul 1988 A
4759769 Hedman et al. Jul 1988 A
4834757 Brantigan May 1989 A
4863477 Monson Sep 1989 A
4904261 Dove et al. Feb 1990 A
4917704 Frey et al. Apr 1990 A
4932969 Frey et al. Jun 1990 A
4946378 Hirayama et al. Aug 1990 A
4997432 Keller Mar 1991 A
5035716 Downey Jul 1991 A
5057108 Shetty et al. Oct 1991 A
5071437 Steffee Dec 1991 A
5122130 Keller Jun 1992 A
5192327 Brantigan Mar 1993 A
5195526 Michelson Mar 1993 A
5258031 Salib et al. Nov 1993 A
5282861 Kaplan Feb 1994 A
5306308 Gross et al. Apr 1994 A
5314477 Marnay May 1994 A
5320644 Baumgartner Jun 1994 A
5370697 Baumgartner Dec 1994 A
5394457 Leibinger et al. Feb 1995 A
5401269 Buttner-Janz et al. Mar 1995 A
5415704 Davidson May 1995 A
5423816 Lin Jun 1995 A
5458642 Beer et al. Oct 1995 A
5462575 Del Corso Oct 1995 A
5484437 Michelson Jan 1996 A
5489307 Kuslich et al. Feb 1996 A
5505732 Michelson Apr 1996 A
5507816 Bullivant Apr 1996 A
5534030 Navarro et al. Jul 1996 A
5556431 Buttner-Janz Sep 1996 A
5674296 Bryan et al. Oct 1997 A
5676701 Yuan et al. Oct 1997 A
5676702 Ratron Oct 1997 A
5683465 Shinn et al. Nov 1997 A
5702450 Bisserie Dec 1997 A
5709683 Bagby Jan 1998 A
5728159 Stroever et al. Mar 1998 A
5741253 Michelson Apr 1998 A
5776198 Rabbe et al. Jul 1998 A
5782832 Larsen et al. Jul 1998 A
5797909 Michelson Aug 1998 A
5797917 Boyd et al. Aug 1998 A
5824094 Serhan et al. Oct 1998 A
5836948 Zucherman et al. Nov 1998 A
5865846 Bryan et al. Feb 1999 A
5865848 Baker Feb 1999 A
5888226 Rogozinski Mar 1999 A
5895428 Berry Apr 1999 A
5899901 Middleton May 1999 A
5899911 Carter May 1999 A
5928284 Mehdizadeh Jul 1999 A
5989251 Nichols Nov 1999 A
5989291 Ralph et al. Nov 1999 A
6001130 Bryan et al. Dec 1999 A
6019792 Cauthen Feb 2000 A
6022376 Assell et al. Feb 2000 A
6039761 Li et al. Mar 2000 A
6039763 Shelokov Mar 2000 A
6080155 Michelson Jun 2000 A
6083228 Michelson Jul 2000 A
6086613 Camino et al. Jul 2000 A
6096038 Michelson Aug 2000 A
6106557 Robioneck et al. Aug 2000 A
6132465 Ray et al. Oct 2000 A
6136031 Middleton Oct 2000 A
6139551 Michelson et al. Oct 2000 A
6139579 Steffee et al. Oct 2000 A
6143033 Paul et al. Nov 2000 A
6146421 Gordon et al. Nov 2000 A
6156067 Bryan et al. Dec 2000 A
6159211 Boriani et al. Dec 2000 A
6159214 Michelson Dec 2000 A
6162252 Kuras et al. Dec 2000 A
6174311 Branch et al. Jan 2001 B1
6176881 Schar et al. Jan 2001 B1
6193757 Foley et al. Feb 2001 B1
6224595 Michelson May 2001 B1
6224607 Michelson May 2001 B1
6231609 Mehdizadeh May 2001 B1
6235030 Zucherman et al. May 2001 B1
6261296 Aebi et al. Jul 2001 B1
6264695 Stoy Jul 2001 B1
6290726 Pope et al. Sep 2001 B1
6296664 Middleton Oct 2001 B1
6315797 Middleton Nov 2001 B1
6322567 Mittelstadt et al. Nov 2001 B1
6336941 Subba Rao et al. Jan 2002 B1
6348071 Steffee et al. Feb 2002 B1
6368350 Erickson et al. Apr 2002 B1
6368351 Glenn et al. Apr 2002 B1
6375681 Truscott Apr 2002 B1
6375682 Fleischmann et al. Apr 2002 B1
6395032 Gauchet May 2002 B1
6402785 Zdeblick et al. Jun 2002 B1
6409766 Brett Jun 2002 B1
6413278 Marchosky Jul 2002 B1
6416551 Keller Jul 2002 B1
6436098 Michelson Aug 2002 B1
6440139 Michelson Aug 2002 B2
6447544 Michelson Sep 2002 B1
6478800 Fraser et al. Nov 2002 B1
6517544 Michelson Feb 2003 B1
6517580 Ramadan et al. Feb 2003 B1
6520967 Cauthen Feb 2003 B1
6520996 Manasas et al. Feb 2003 B1
6527804 Gauchet et al. Mar 2003 B1
6533817 Norton et al. Mar 2003 B1
6537279 Michelson Mar 2003 B1
6554863 Paul et al. Apr 2003 B2
6562047 Ralph et al. May 2003 B2
6562074 Gerbec et al. May 2003 B2
6565574 Michelson May 2003 B2
6579321 Gordon et al. Jun 2003 B1
6582466 Gauchet Jun 2003 B1
6582468 Gauchet Jun 2003 B1
6592624 Fraser et al. Jul 2003 B1
6599294 Fuss et al. Jul 2003 B2
6607558 Kuras Aug 2003 B2
6607559 Ralph et al. Aug 2003 B2
6610092 Ralph et al. Aug 2003 B2
6623525 Ralph et al. Sep 2003 B2
6645248 Casutt Nov 2003 B2
6648895 Burkus et al. Nov 2003 B2
6652533 O'Neil Nov 2003 B2
6660038 Boyer, II et al. Dec 2003 B2
6666866 Martz et al. Dec 2003 B2
6669731 Ralph et al. Dec 2003 B2
6669732 Serhan et al. Dec 2003 B2
6673113 Ralph et al. Jan 2004 B2
6682562 Viart et al. Jan 2004 B2
6689132 Biscup Feb 2004 B2
6706068 Ferree Mar 2004 B2
6709439 Rogers et al. Mar 2004 B2
6712819 Zucherman et al. Mar 2004 B2
6712825 Aebi et al. Mar 2004 B2
6719794 Gerber et al. Apr 2004 B2
6723097 Fraser et al. Apr 2004 B2
6726720 Ross et al. Apr 2004 B2
6726721 Stoy et al. Apr 2004 B2
6733532 Gauchet et al. May 2004 B1
6740118 Eisermann et al. May 2004 B2
6740119 Ralph et al. May 2004 B2
6752832 Neumann Jun 2004 B2
6755841 Fraser et al. Jun 2004 B2
6764512 Keller Jul 2004 B2
6764515 Ralph et al. Jul 2004 B2
6770095 Grinberg et al. Aug 2004 B2
6790233 Brodke et al. Sep 2004 B2
6793678 Hawkins Sep 2004 B2
6814737 Cauthen Nov 2004 B2
6821298 Jackson Nov 2004 B1
6827740 Michelson Dec 2004 B1
6830570 Frey et al. Dec 2004 B1
6835206 Jackson Dec 2004 B2
6846328 Cauthen Jan 2005 B2
6852126 Ahlgren Feb 2005 B2
6863673 Gerbec et al. Mar 2005 B2
6875213 Michelson Apr 2005 B2
6896680 Michelson May 2005 B2
6899735 Coates et al. May 2005 B2
6936071 Marnay et al. Aug 2005 B1
6936132 Topolnitsky Aug 2005 B2
6964686 Gordon Nov 2005 B2
6966929 Mitchell Nov 2005 B2
6966931 Huang Nov 2005 B2
6986788 Paul et al. Jan 2006 B2
6989011 Paul et al. Jan 2006 B2
6994727 Khandkar et al. Feb 2006 B2
7011684 Eckman Mar 2006 B2
7022138 Mashburn Apr 2006 B2
7025787 Bryan et al. Apr 2006 B2
7044972 Mathys et al. May 2006 B2
7044983 Cheng May 2006 B1
7056344 Huppert et al. Jun 2006 B2
7060073 Frey et al. Jun 2006 B2
7066958 Ferree Jun 2006 B2
7081120 Li et al. Jul 2006 B2
7083651 Diaz et al. Aug 2006 B2
7087055 Lim et al. Aug 2006 B2
7097648 Globerman et al. Aug 2006 B1
7115132 Errico et al. Oct 2006 B2
7118580 Beyersdorff et al. Oct 2006 B1
7147665 Bryan et al. Dec 2006 B1
7153325 Kim et al. Dec 2006 B2
7169182 Errico et al. Jan 2007 B2
7179294 Eisermann et al. Feb 2007 B2
7182784 Evans et al. Feb 2007 B2
7198644 Schultz et al. Apr 2007 B2
7207991 Michelson Apr 2007 B2
7214244 Zubok et al. May 2007 B2
7217291 Zucherman et al. May 2007 B2
7235082 Bartish et al. Jun 2007 B2
7235101 Berry et al. Jun 2007 B2
7235103 Rivin Jun 2007 B2
7250060 Trieu Jul 2007 B2
7255714 Malek Aug 2007 B2
7261739 Ralph et al. Aug 2007 B2
7267688 Ferree Sep 2007 B2
7270679 Istephanous et al. Sep 2007 B2
7270682 Frigg et al. Sep 2007 B2
7303582 Brady Dec 2007 B2
7303583 Schär et al. Dec 2007 B1
7309358 Berry et al. Dec 2007 B2
7318839 Malberg et al. Jan 2008 B2
7326250 Beaurain et al. Feb 2008 B2
7331994 Gordon Feb 2008 B2
7331995 Eisermann et al. Feb 2008 B2
7429270 Baumgartner et al. Sep 2008 B2
7442211 de Villiers et al. Oct 2008 B2
7452380 Zubok et al. Nov 2008 B2
7491241 Errico et al. Feb 2009 B2
7494508 Zeegers Feb 2009 B2
7517363 Rogers et al. Apr 2009 B2
7531001 de Villiers et al. May 2009 B2
7549995 Schultz et al. Jun 2009 B2
7563284 Coppes et al. Jul 2009 B2
7563286 Gerber et al. Jul 2009 B2
7575598 Albert et al. Aug 2009 B2
7578848 Albert et al. Aug 2009 B2
7585324 Albert et al. Sep 2009 B2
7585326 de Villiers et al. Sep 2009 B2
7615078 White et al. Nov 2009 B2
7635368 Errico et al. Dec 2009 B2
7637913 de Villiers et al. Dec 2009 B2
7655045 Richelsoph Feb 2010 B2
7708776 Blain et al. May 2010 B1
7708777 O'Neil et al. May 2010 B2
7731753 Reo et al. Jun 2010 B2
7731754 de Villiers et al. Jun 2010 B2
7749272 Robie et al. Jul 2010 B2
7763055 Foley Jul 2010 B2
7819922 Sweeney Oct 2010 B2
8057545 Hughes et al. Nov 2011 B2
8092534 Eckhardt Jan 2012 B2
8142505 Tauber Mar 2012 B2
8298287 Moumene Oct 2012 B2
8491637 Matthis Jul 2013 B2
8758441 Hovda et al. Jun 2014 B2
8771357 Biedermann Jul 2014 B2
20010016773 Serhan et al. Aug 2001 A1
20010029377 Aebi et al. Oct 2001 A1
20010051829 Middleton Dec 2001 A1
20020022845 Zdeblick et al. Feb 2002 A1
20020035400 Bryan et al. Mar 2002 A1
20020045904 Fuss et al. Apr 2002 A1
20020068936 Burkus et al. Jun 2002 A1
20020091392 Michelson Jul 2002 A1
20020116009 Fraser et al. Aug 2002 A1
20020123753 Michelson Sep 2002 A1
20020128715 Bryan et al. Sep 2002 A1
20020165550 Frey et al. Nov 2002 A1
20020177897 Michelson Nov 2002 A1
20020198532 Michelson Dec 2002 A1
20030009224 Kuras Jan 2003 A1
20030014116 Ralph et al. Jan 2003 A1
20030023245 Ralph et al. Jan 2003 A1
20030028249 Baccelli et al. Feb 2003 A1
20030040746 Mitchell et al. Feb 2003 A1
20030045884 Robie et al. Mar 2003 A1
20030045939 Casutt Mar 2003 A1
20030074076 Ferree Apr 2003 A1
20030083747 Winterbottom et al. May 2003 A1
20030100951 Serhan et al. May 2003 A1
20030125739 Bagga Jul 2003 A1
20030130662 Michelson Jul 2003 A1
20030135277 Bryan et al. Jul 2003 A1
20030139812 Garcia et al. Jul 2003 A1
20030187448 Michelson Oct 2003 A1
20030191536 Ferree Oct 2003 A1
20030195517 Michelson Oct 2003 A1
20030195631 Ferree Oct 2003 A1
20030199982 Bryan Oct 2003 A1
20030199983 Michelson Oct 2003 A1
20030204261 Eisermann et al. Oct 2003 A1
20030208271 Kuras Nov 2003 A1
20030229358 Errico et al. Dec 2003 A1
20030233145 Landry et al. Dec 2003 A1
20040002761 Rogers et al. Jan 2004 A1
20040024407 Ralph Feb 2004 A1
20040024410 Olson et al. Feb 2004 A1
20040030391 Ferree Feb 2004 A1
20040034426 Errico et al. Feb 2004 A1
20040054411 Kelly et al. Mar 2004 A1
20040059318 Zhang et al. Mar 2004 A1
20040073307 Keller Apr 2004 A1
20040073311 Ferree Apr 2004 A1
20040073312 Eisermann et al. Apr 2004 A1
20040093087 Ferree et al. May 2004 A1
20040097928 Zdeblick et al. May 2004 A1
20040098131 Bryan et al. May 2004 A1
20040117021 Biedermann et al. Jun 2004 A1
20040143270 Zucherman et al. Jul 2004 A1
20040143332 Krueger et al. Jul 2004 A1
20040143334 Ferree Jul 2004 A1
20040167626 Geremakis et al. Aug 2004 A1
20040176843 Zubok et al. Sep 2004 A1
20040186569 Berry Sep 2004 A1
20040215342 Suddaby Oct 2004 A1
20040225295 Zubok et al. Nov 2004 A1
20040225365 Eisermann et al. Nov 2004 A1
20040230307 Eisermann et al. Nov 2004 A1
20040236426 Ralph et al. Nov 2004 A1
20040243238 Arin et al. Dec 2004 A1
20040254644 Taylor Dec 2004 A1
20050015094 Keller Jan 2005 A1
20050015095 Keller Jan 2005 A1
20050015152 Sweeney Jan 2005 A1
20050021145 de Villiers et al. Jan 2005 A1
20050021146 de Villiers et al. Jan 2005 A1
20050027360 Webb et al. Feb 2005 A1
20050038515 Kunzler Feb 2005 A1
20050043800 Paul et al. Feb 2005 A1
20050085917 Marnay et al. Apr 2005 A1
20050107881 Alleyne et al. May 2005 A1
20050113842 Bertagnoli et al. May 2005 A1
20050113928 Cragg May 2005 A1
20050143824 Richelsoph et al. Jun 2005 A1
20050149189 Mokhtar et al. Jul 2005 A1
20050154463 Trieu Jul 2005 A1
20050165408 Puno et al. Jul 2005 A1
20050171604 Michalow Aug 2005 A1
20050187634 Berry Aug 2005 A1
20050192586 Zucherman et al. Sep 2005 A1
20050192670 Zubok et al. Sep 2005 A1
20050197706 Hovorka et al. Sep 2005 A1
20050216081 Taylor Sep 2005 A1
20050216084 Fleischmann et al. Sep 2005 A1
20050234553 Gordon Oct 2005 A1
20050251260 Gerber et al. Nov 2005 A1
20050251261 Peterman Nov 2005 A1
20050261772 Filippi et al. Nov 2005 A1
20050267580 Suddaby Dec 2005 A1
20050267581 Marnay et al. Dec 2005 A1
20060004377 Keller Jan 2006 A1
20060004453 Bartish et al. Jan 2006 A1
20060015183 Gilbert et al. Jan 2006 A1
20060020342 Ferree et al. Jan 2006 A1
20060025862 Villiers et al. Feb 2006 A1
20060030862 de Villiers et al. Feb 2006 A1
20060036325 Paul et al. Feb 2006 A1
20060041313 Allard et al. Feb 2006 A1
20060041314 Millard Feb 2006 A1
20060052870 Feree Mar 2006 A1
20060064169 Feree et al. Mar 2006 A1
20060069439 Zucherman et al. Mar 2006 A1
20060116768 Krueger et al. Jun 2006 A1
20060136061 Navarro et al. Jun 2006 A1
20060142858 Colleran Jun 2006 A1
20060142862 Diaz et al. Jun 2006 A1
20060155378 Eckman Jul 2006 A1
20060167549 Mathys et al. Jul 2006 A1
20060178744 de Villiers et al. Aug 2006 A1
20060178746 Bartish, Jr. et al. Aug 2006 A1
20060195097 Evans et al. Aug 2006 A1
20060200239 Rothman et al. Sep 2006 A1
20060200240 Rothman et al. Sep 2006 A1
20060200242 Rothman et al. Sep 2006 A1
20060200243 Rothman Sep 2006 A1
20060224241 Butler et al. Oct 2006 A1
20060235426 Lim et al. Oct 2006 A1
20060235525 Gil et al. Oct 2006 A1
20060235527 Buettner-Janz et al. Oct 2006 A1
20060241641 Albans et al. Oct 2006 A1
20060241766 Felton et al. Oct 2006 A1
20060259144 Trieu Nov 2006 A1
20060259146 Navarro et al. Nov 2006 A1
20060265068 Schwab Nov 2006 A1
20060265077 Zwirkoski Nov 2006 A1
20060276902 Zipnick et al. Dec 2006 A1
20060287728 Mokhtar et al. Dec 2006 A1
20060293752 Moumene et al. Dec 2006 A1
20060293753 Thramann Dec 2006 A1
20060293754 de Villiers et al. Dec 2006 A1
20070010826 Rhoda et al. Jan 2007 A1
20070021837 Ashman et al. Jan 2007 A1
20070032875 Blacklock et al. Feb 2007 A1
20070067035 Falahee Mar 2007 A1
20070067036 Hudgins et al. Mar 2007 A1
20070073398 Fabian et al. Mar 2007 A1
20070093898 Schwab et al. Apr 2007 A1
20070100453 Parsons et al. May 2007 A1
20070100454 Burgess et al. May 2007 A1
20070100456 Dooris et al. May 2007 A1
20070123903 Raymond et al. May 2007 A1
20070123904 Stad et al. May 2007 A1
20070135923 Peterman et al. Jun 2007 A1
20070162133 Doubler et al. Jul 2007 A1
20070168033 Kim et al. Jul 2007 A1
20070168036 Ainsworth et al. Jul 2007 A1
20070179615 Heinz et al. Aug 2007 A1
20070213821 Kwak et al. Sep 2007 A1
20070233077 Khalili Oct 2007 A1
20070233247 Schwab Oct 2007 A1
20070233248 Schwab et al. Oct 2007 A1
20070233251 Abdou Oct 2007 A1
20070270956 Heinz Nov 2007 A1
20070270970 Trieu Nov 2007 A1
20070282449 de Villiers et al. Dec 2007 A1
20070299521 Glenn et al. Dec 2007 A1
20080015698 Marino et al. Jan 2008 A1
20080015701 Garcia et al. Jan 2008 A1
20080021557 Trieu Jan 2008 A1
20080051900 de Villiers et al. Feb 2008 A1
20080051901 de Villiers et al. Feb 2008 A1
20080125864 de Villiers et al. May 2008 A1
20080125865 Abdelgany May 2008 A1
20080133011 de Villiers et al. Jun 2008 A1
20080154301 de Villiers et al. Jun 2008 A1
20080154305 Foley et al. Jun 2008 A1
20080154382 de Villiers et al. Jun 2008 A1
20080161926 Melkent et al. Jul 2008 A1
20080215155 de Villiers et al. Sep 2008 A1
20080221696 de Villiers et al. Sep 2008 A1
20080228274 de Villiers et al. Sep 2008 A1
20080228277 de Villiers et al. Sep 2008 A1
20080294259 de Villiers et al. Nov 2008 A1
20090043391 de Villiers et al. Feb 2009 A1
20090048674 Zubok et al. Feb 2009 A1
20090048677 McLeod et al. Feb 2009 A1
20090076614 Arramon Mar 2009 A1
20090105833 Hovda et al. Apr 2009 A1
20090105834 Hovda et al. Apr 2009 A1
20090105835 Hovda et al. Apr 2009 A1
20090118836 Cordaro May 2009 A1
20090192617 Arramon et al. Jul 2009 A1
20090205188 de Villiers et al. Aug 2009 A1
20090210060 de Villiers et al. Aug 2009 A1
20090222101 de Villiers et al. Sep 2009 A1
20090276051 Arramon et al. Nov 2009 A1
20090326656 de Villiers et al. Dec 2009 A1
20100004746 Arramon Jan 2010 A1
20100004748 Cordaro Jan 2010 A1
20100016972 Jansen et al. Jan 2010 A1
20100016973 de Villiers et al. Jan 2010 A1
20100030335 Arramon Feb 2010 A1
20100049040 de Villiers et al. Feb 2010 A1
20100069976 de Villiers et al. Mar 2010 A1
20100076558 de Villiers et al. Mar 2010 A1
20100087868 Barr et al. Apr 2010 A1
20100100141 de Villiers et al. Apr 2010 A1
20100179419 de Villiers et al. Jul 2010 A1
20100268344 de Villiers et al. Oct 2010 A1
20170071757 Hovda et al. Mar 2017 A1
Foreign Referenced Citations (52)
Number Date Country
3023353 Apr 1981 DE
3023353 Apr 1981 DE
10035182 Feb 2002 DE
0333990 Sep 1989 EP
0333990 May 1990 EP
0560140 Sep 1993 EP
0560141 Sep 1993 EP
0591712 Apr 1994 EP
0820740 Jan 1998 EP
1142544 Oct 2001 EP
1153582 Nov 2001 EP
1153582 Nov 2001 EP
1250898 Oct 2002 EP
1306064 May 2003 EP
1344493 Sep 2003 EP
1344506 Sep 2003 EP
1344507 Sep 2003 EP
1344508 Sep 2003 EP
1417940 May 2004 EP
1570813 Sep 2005 EP
2803741 Jul 2001 FR
61122859 Jun 1986 JP
S61122859 Jun 1986 JP
63164948 Jul 1988 JP
S63164948 Jul 1988 JP
WO-9920209 Apr 1999 WO
WO-9930651 Jun 1999 WO
WO-0004851 Feb 2000 WO
WO-0035384 Jun 2000 WO
WO-0042954 Jul 2000 WO
WO-0042954 Nov 2000 WO
WO-0101893 Jan 2001 WO
WO-0115637 Mar 2001 WO
WO-0168003 Sep 2001 WO
WO-0211650 Feb 2002 WO
WO-0211650 Sep 2003 WO
WO-2004000170 Dec 2003 WO
WO-2004000171 Dec 2003 WO
WO-2004026187 Apr 2004 WO
WO-2004054477 Jul 2004 WO
WO-2005004756 Jan 2005 WO
WO-2005004756 May 2005 WO
WO-2005053580 Jun 2005 WO
WO-2005072662 Aug 2005 WO
WO-2005112834 Dec 2005 WO
WO-2005112834 May 2006 WO
WO-2006119092 Nov 2006 WO
WO-2006119092 Dec 2006 WO
WO-2007121320 Oct 2007 WO
WO-2007121320 Jun 2008 WO
20039312 Nov 2003 ZA
200603171 Sep 2007 ZA
Non-Patent Literature Citations (21)
Entry
Chadwick et al., Radiolucent Structural Materials for Medical Applications, Jun. 1, 2001, MDDI, p. 1, http://www.mddionline.com/article/radiolucent-structural-materials-medical-applications.
Office action dated Feb. 8, 2012 for U.S. Appl. No. 12/255,731.
Office action dated Apr. 18, 2012 for U.S. Appl. No. 12/255,733.
Office action dated Jun. 7, 2011 for U.S. Appl. No. 12/255,731.
Office action dated Aug. 26, 2011 for U.S. Appl. No. 12/255,733.
Office action dated Nov. 23, 2012 for U.S. Appl. No. 12/255,731.
Office action dated Nov. 28, 2012 for U.S. Appl. No. 12/255,733.
“ffice Action dated Dec. 19, 2017 for U.S. Appl. No. 15/359,298”.
International search report and written opinion dated Dec. 16, 2008 for PCT/US2008/080800.
Office action dated May 13, 2011 for U.S. Appl. No. 12/255,737.
Office action dated Jun. 19, 2012 for U.S. Appl. No. 12/255,737.
Office action dated Dec. 15, 2011 for U.S. Appl. No. 12/255,737.
Office action dated Dec. 18, 2012 for U.S. Appl. No. 12/255,737.
International Search Report and Written Opinion of PCT Application No. PCT/US08/80800, dated Dec. 16, 2008, 11 pages total.
Buttner-Janz, The Development of.the Artificial Disc. Introduction, pp. 1-18, Library of Congress Catalogue No. 92-75582, ISBN 0-9635430-0-8 (1989).
Hellier, et al. Wear Studies for Development of an Intervertebral Disc Prosthesis. Spine, vol. 17 No. 6 Supplement pp. 86-96 (1992).
International search report and written opinion dated Dec. 19, 2008 for PCT/US2008/080798.
International search report and written opinion dated Dec. 29, 2008 for PCT/US2008/080804.
Lee, et al. Impact Response of the Intervertebral Disc in a Finite-Element Model. Spine. 2000; 25(19):2431-2439.
Lehuec, et al. Shock Absorption in Lumber Disc Prosthesis. Journal of Spinal Disorders & Techniques. 2003; 16(4):346-351.
Office action dated Aug. 14, 2013 for U.S. Appl. No. 12/255,731.
Provisional Applications (1)
Number Date Country
60981665 Oct 2007 US
Reissues (1)
Number Date Country
Parent 12255737 Oct 2008 US
Child 15191385 US