The present application is directed to implants, devices and methods for stabilizing vertebral members, and more particularly, to intervertebral implants, devices and methods of use in replacing an intervertebral disc, a vertebral member, or a combination of both to distract and/or stabilize the spine.
The spine is divided into four regions comprising the cervical, thoracic, lumbar, and sacrococcygeal regions. The cervical region includes the top seven vertebral members identified as C1-C7. The thoracic region includes the next twelve vertebral members identified as T1-T12. The lumbar region includes five vertebral members L1-L5. The sacrococcygeal region includes nine fused vertebral members that form the sacrum and the coccyx. The vertebral members of the spine are aligned in a curved configuration that includes a cervical curve, thoracic curve, and lumbosacral curve. Intervertebral discs are positioned between the vertebral members and permit flexion, extension, lateral bending, and rotation.
As is known, various conditions and ailments may lead to damage of the spine, intervertebral discs and/or the vertebral members. The damage may result from a variety of causes including, but not limited to, events such as trauma, a degenerative condition, a tumor, or infection. Damage to the intervertebral discs and vertebral members can lead to pain, neurological deficit, and/or loss of motion.
Various procedures include replacing a section of or the entire vertebral member, a section of or the entire intervertebral disc, or both. One or more replacement implants may be inserted to replace the damaged vertebral members and/or discs. The implants are configured to be inserted into the intervertebral space and contact against adjacent vertebral members. The implants are intended to reduce or eliminate the pain and neurological deficit, and increase the range of motion.
The curvature of the spine and general shapes of the vertebral members may make it difficult for the implants to adequately contact the adjacent vertebral members or to position the adjacent vertebral members in a desired orientation. There is thus a need for implants or devices configurable to match the spinal anatomy for secure contact and/or desired orientation when implanted into an intervertebral space.
The present application discloses implants or devices for insertion into an intervertebral space between first and second vertebral members, the implant comprising an implant body with at least one base section having positioning teeth, and an end cap adapted for selective positioning at a selected point on the base section. The end cap comprises a seating surface adapted to contact the base section when the end cap is positioned on the implant body, an end cap angulation, and at least one positioning passage adapted to receive the positioning teeth. The positioning passages and positioning teeth are complementarily configured to facilitate slideably positioning the end cap on the base section. And, at least one of the positioning passages comprises a resilient locking tenon adapted to deflect as a positioning tooth slideably travels in the at least one positioning passage such that the positioning tooth is lockingly engaged by the locking tenon in the at least one of the positioning passage. The implant body and end cap combination will impart end cap angulation to an adjacent vertebral body at the selected point when the implant is positioned in the intervertebral space. The end cap can be selectively positioned at the selected point on the base section via adjustment of an end cap approach direction. The implant may further comprise a locking mechanism adapted to lockingly engage the end cap and base section and prevent axial movement of the end cap relative to the implant base section. The implant may also comprise an end cap height measured relative to the seating surface which enables the implant to both impart end cap height and end cap angulation to the adjacent vertebral body at the selected point.
There is also provided an implant for insertion into an intervertebral space between a first and second vertebral member comprising an implant body with at least one base section having positioning teeth, an end cap adapted for selective positioning at a selected point on the base section, and a locking mechanism adapted to locking engage the end cap to the base section. The end cap comprises a seating surface adapted to contact the base section when the end cap is positioned on the implant body, an end cap angulation, and positioning passages adapted to slideably receive aligned positioning teeth therein. The positioning passages and positioning teeth are complementarily configured to facilitate slideably positioning the end cap on the base section. And, at least one of the positioning passages comprising a resilient locking tenon having a tooth holding surface, the locking tenon adapted to deflect as a positioning tooth slideably travels in the positioning passage such that the positioning tooth is lockingly engaged by the tooth holding surface in the at least one of the positioning passage. The implant body and end cap combination will impart the end cap angulation to an adjacent vertebral body at the selected point when the implant is positioned in the intervertebral space. The end cap is selectively positioned at the selected point on the base section via adjustment of an end cap approach direction. The implant locking mechanism is further adapted to prevent axial movement of the end cap relative to the implant base section. The implant may also comprise an end cap height measured relative to the seating surface which enables the implant to both impart end cap height and end cap angulation to the adjacent vertebral body at the selected point.
The various aspects of the various embodiments may be used alone or in any combination, as is desired.
The present application is directed to intervertebral implants for spacing apart vertebral members 100 and 105.
As shown in
The implant body 20 is configured to slideably receive an end cap 40 or 42 at the first and second base sections 15 and 25, respectively, from a substantially lateral and perpendicular direction to the implant's longitudinal axis 5. The inner implant body 22 includes a first base section 15 with positioning teeth or spikes 30. The positioning teeth or spikes 30 are positioned substantially about the periphery of the first base section 15 and extend away from an exterior surface 16 of the first base section 15 in a substantially vertical or axial direction. The outer implant body 24 includes a second base section 25 with similar positioning teeth or spikes 30. The positioning teeth or spikes 30 are positioned substantially about the periphery of the second base section 25 and extend away from an exterior surface 26 of the first base section 15 in a substantially vertical or axial direction.
The implant base section 15 and 25 includes base apertures 17A and 17B, shown in
The implant base section 15 and 25 comprises two or more positioning teeth or spikes 30 to accept and provide for slideable placement, positioning and engaging of the end cap 40 or 42 onto the implant base section 15 and 25 as shown in
The positioning teeth 30 enable the end cap 40 or 42 to be inserted into and slideably travel inside the end cap 40 or 42 via corresponding and complementary configured positioning passages or end cap slots 31 or 35. The positioning passages 31 or 35 are preferably end cap slots complementarily shaped and configured to permit the positioning teeth 30 to enter and slideably travel therein. The positioning teeth 30 are also adapted to engage and interlock with the corresponding and complementary positioning passages or end cap slots 31 or 35 to form an end cap locking mechanism 50, shown in
In one aspect, shown in
With respect to the interior end cap slots 31, as the end cap 40 or 42 slideably travels over and across the exterior surface 16 or 26 of the implant base section 15 or 25, the positioning teeth 30 enter and engage the interior positioning passages or end cap slots 31, and thereafter slideably travel in the interior end cap slots 31. The interior positioning passages or interior end cap slots 31, via the substantially arrow-shaped aperture and slot shoulder walls 27, which will engage and interact with the positioning teeth 30 at the positioning teeth heads 29 and tooth base 28 as the positioning teeth 30 travel in the interior exterior end cap slots 31. The positioning teeth bases 28, which are narrow relative to the teeth heads 29 in this embodiment, will slideably engage and travel along lateral end cap slot shoulder walls 27 and across a narrow slot area 31B, best shown in
The positioning teeth 30 will slideably travel inside the end cap slots 31 and 35 until the end cap 40 or 42 reaches a desired or selected final end cap position on the implant base section 15, or as discussed below, until the positioning teeth 30 in the exterior end cap slots 35 reach and abut up against a corresponding exterior positioning passage slot wall 33. The positioning teeth 30 may also slideably travel inside the end cap slots 31 and 35 until the end cap 40 or 42 reaches another desired or selected end cap position on the implant base section 15. As the end cap 40 or 42 is moved or forced to slideably travel over or across the implant base section 15 or 25, the positioning teeth 30 will slideably travel inside the end cap slots 31.
The arrow shaped aperture of the interior end cap slots 31 is preferably and complimentarily sized such that, at the final or desired end cap position, e.g., as shown in
The holding strength of the friction fit between the positioning teeth 30 and interior end cap slots 31 may be augmented or controlled by the addition or use of a coating substance between the interior end cap slots 31 and the positioning teeth 30. For example, a coating, such a silicone, may be used to increase friction between the interior end cap slots 31 and the positioning teeth 30. Those of skill in the art will recognize that other substances or friction control mechanism may be used to augment or control friction strength between the interior end cap slots 31 and the positioning teeth 30.
With respect to the exterior end cap slots 35, as the end cap 40 or 42 slideably travels over and across the exterior surface 16 or 26 of the implant base section 15 or 25, the positioning teeth 30 also enter and engage the exterior positioning passages or end cap slots 35, and thereafter slideably travel in the exterior end cap slots 35 between the locking tenon 36 and lateral wall 38. As the positioning teeth 30 continues to travel in the exterior end cap slots 35, the positioning teeth 30 will encounter a tooth holding surface 39 which extends interiorly from the locking tenon 36. As the positioning teeth 30 continue to travel they will impart an outward force on the tooth holding surface 39 and by extension the locking tenon 36. If the imparted outward force is sufficient to overcome the tendency or physical properties which maintain the deflecting tenon in an initial equilibrium position, then the positioning tooth 30 will force the locking tenon 36 to deflect or flex outwardly away from its initial equilibrium position. The locking tenon's 36 deflection outwardly moves the tooth holding surface 39 which in turn permits the positioning tooth 30 to continue its sliding travel into the exterior end cap slot 35. When the positioning teeth 30 slideably travels past the tooth holding surface 39, the outward force being imparted by the positioning teeth's 30 on the locking tenon 36 is removed. With the outward force removed, the deflecting tenon's resilient or spring-like properties will force or bias the locking tenon 36 back towards its initial equilibrium position and move the locking tenon 36 back in an inward direction toward a locking equilibrium position. The initial and locking equilibrium positions may or may not be the same deflecting tenon positions.
Once the positioning teeth 30 travels past the tooth holding surface 39, in the embodiment shown in
In the locking position, the locking tenon 36 and exterior positioning passage slot wall 33 provide a holding force or fit on the positioning teeth 30, translated to the positioning teeth 30 by the tooth holding surface 39 and exterior positioning passage slot wall 33. The positioning teeth 30 will remain in the locked position until sufficient force is applied to overcome the deflecting tenon's holding force and permit slideable removal of the end cap 40 or 42. When such removal force is provided to the end cap 40 or 42, the locking tenon 36 and tooth holding surface 39 will move outwardly and thereby permit the positioning teeth 30 to slideably travel out of the exterior end cap slots 35. The holding strength or force provided by the locking tenon 36 may be augmented or controlled by selection and use of different tenon materials with different resilient physical properties, or through the use of coating substances between the tooth holding surface 39 and the positioning teeth 30. For example, a coating, such as silicone, may be used to increase friction between the tooth holding surface 39 and the positioning teeth 30. Those of skill in the art will recognize that other substances or friction control mechanisms and material may be used to augment or control the holding force or strength and friction between the tooth holding surface 39 and the positioning teeth 30.
Additionally, the positioning teeth 30 and complementary positioning passages or end cap slots 31 cooperatively engage and interact to prevent movement or travel of the end cap 40 or 42 in an axial direction along the implant axis 5 relative to the first or second base section 15 or 25. In particular, in the disclosed embodiment shown in
Once the end cap 40 or 42 is at a desired or selected approach direction and orientation XY (e.g., at XY1 or XY1′), the end cap 40 or 42 can be positioned on the implant base section 15 or 25. The end cap 40 and 42 is moved to approach the implant base section 15 or 25 from a respective direction and orientation XY1 and XY1′ that is substantially perpendicular to the implant's longitudinal axis 5 and parallel to the respective exterior surface 16 or 26, which permits the end cap 40 and 42 to be slideably positioned on the respective exterior surface 16 or 26 of the implant base section 15 or 25. The complementary positioning teeth 30 and positioning passages 31 enable the end cap 40 and 42 to be slideably positioned on the respective implant base section 15 or 25.
As the first end 32 of the end caps 40 or 42 approaches the implant base section 15 or 25, the positioning passages or end cap slots 31 and 35 permit the positioning teeth 30 to enter the end cap slots 31 and 35, which in turn permit the end cap 40 or 42 to slideably travel over and across the exterior surfaces 16 or 26 of the implant base sections 15 or 25. The positioning teeth 30 are configured to slideably travel inside the positioning passages or end cap slots 31 and 35 as the end cap 40 or 42 is actively moved or forced over and across the exterior surface 16 or 26. So long as the end cap 40 or 42 is actively moved or forced over and across the exterior surface 16 or 26, the positioning teeth 30 will continue to slideably travel inside the end cap slots 31 and 35 until the end cap 40 or 42 reaches a desired end cap position on the implant base section 15 or 25, as described above in discussing interior and exterior end cap slots 31 and 35. The desired end cap position on the implant base section 15 or 25 can be selected by a physician or may be selected to meet, or dictated by, medical or surgical needs. The desired end cap position may be a final end cap position where the end cap 40 or 42 is centered and aligned with the implant's axis 5, as shown in
As discussed above, the positioning teeth 30 can also slideably travel inside the exterior end cap slots 35 until at least one positioning tooth 30 reaches and abuts up against a corresponding positioning passage wall or slot wall 33 located at or about an opposing second end 34 of the end cap 40 or 42, as shown in
Those of skill in the art will recognize further, that in other aspects, it may be advantageous to have an end cap 40 or 42 with all positioning passages or end cap slots 31 and 35 that do not have corresponding positioning passage rear slot walls 33. In such an aspect, as the end cap 40 or 42 is actively moved across the implant base section 15 or 25, the positioning teeth 30 will continue to slideably travel inside the end cap slots 31 and 35. If the end cap 40 or 42 continues to be slideably moved across the exterior surface 16 or 26, such that the end cap's opposing second end 34 travels past the starting point where the end cap first end 32 initially traveled over the implant base section 15 or 25, then the end cap's first end 32 will travel completely across and past the implant base section 40 or 42. And further, if the end cap 40 or 42 continues to be moved slideably across the implant base section 15 or 25, the end cap's opposing second end 34 will continue to travel across the implant base section 15 or 25 until the end cap's second end 34 too will have traveled completely across and past the implant base section 15 or 25. At this point, the end cap 40 or 42 would be separate from the implant base section 15 or 25 since it has now traveled completely across and past the implant base section 40 or 42. The final end cap position on the implant base section 15 or 25 in such an aspect will be selected by a physician or may be selected to meet, or dictated by, medical or surgical needs.
The contact surface 48 can include end cap teeth or spikes 49 which will engage the end plates of an adjacent vertebral member 100 or 105. The end cap teeth or spikes 49 may be a series of equidistantly spaced end cap teeth or spikes 49 extending from the end cap exterior surface 48, as shown in
The end cap teeth or spikes 49 will come in contact with and engage the end plates of an adjacent vertebral body 100 or 105 once the combined implant body 10 and end cap 40 or 42 are positioned in an intervertebral space 101 between the vertebral members 100 and 105. The end cap teeth or spikes 49 will extend from the end cap exterior surface 48 sufficiently to grip, penetrate and embed into the adjacent vertebral member 100 and 105 end plate to thereby provide implant stability in the intervertebral disc space 101 and prevent the inserted implant 10 from being ejected out of the intervertebral space 101 after implant 10 insertion. The end cap teeth or spikes 49 will provide a securing and stabilizing function of the combined end cap 40 and implant body 10. The actual height of the end cap teeth or spikes 49 can vary to accommodate the selection or need of a surgeon, medical procedure or clinical need. When an implant 10, with positioning base teeth 30 and one or two end caps 40 or 42, is inserted into an intervertebral space 101 and set to a desired implant height, via appropriate instruments (not shown), the protruding end cap teeth or spikes 49 will grip and penetrate into the adjacent vertebral member end plate to maintain a stable implant 10 position between the adjacent vertebral members 100 and 105.
As discussed previously, the end cap 40 or 42 positioning passages or end cap slots 31 and 35 have complementary sliding configurations to the positioning teeth 30 which permit the end cap slots 31 and 35 to engage and interlock and with the plurality of corresponding and complementary shaped positioning teeth 30 when the end cap 40 or 42 is slideably positioned on the implant base section 15 and 25. The positioning passages or end cap slots 31 & 35 and positioning teeth 30 cooperatively interact to form the locking mechanism 50 to lock the end cap 40 or 42 onto the first or second base sections 15 or 25. When the end cap 40 or 42 is positioned on the implant base section 15 or 25, the positioning teeth 30 provide for a stable placement and positioning of the end cap 40 onto the implant base section 15 or 25 via complementary interaction with corresponding end cap slots 31 and 35. The positioning teeth 30, in addition to providing a mechanism to accept placement of the end cap 40 or 42 on the implant base section 15 or 25, provide a securing and stabilizing function so that the end cap 40 or 42 can be securely and slideably positioned on the implant base section 15 and 25.
The end cap 40 or 42 preferably further comprises an angulation aspect θ and an end cap vertex height H. The end cap angulation θ and cap height H may have a range of values as may be selected or needed by a surgeon, medical procedure or clinical application. In one aspect, preferred discrete values for end cap angulation are 0°, 4°, 8° and 15° degrees measured from an angulation reference line X, shown in
As previously discussed, an end cap 40 or 42 preferably comprises one or more positioning passage or end cap slots 31 and 35 which permit sliding insertion of positioning teeth 30 into the positioning passages or end cap slots 31 and 35 when the end cap 40 or 42 is positioned on the implant base section 15 and 25. The positioning passages or end cap slots 31 and 35 are preferably complementarily shaped and configured to permit the positioning teeth 30 to enter and slideably travel inside the end cap slots 31 and 35. The end cap slots 31 and 35 will have a size and configuration which complements the positioning teeth 30 and which permits sliding insertion and locking of the positioning teeth 30 in the end cap slots 31 and 35. Those of skill in the art will recognize that different sizes, shapes and configuration may be used for the positioning passages or end cap slots 31 and 35 and complementary positioning teeth 30 depending on medical procedure or clinical need, or surgeon need or selection, as long as they permit sliding insertion and locking of positioning teeth 30 in the end cap slots 31 when the end cap 40 or 42 is positioned on the implant base section 15 and 25.
As best shown in
The positioning passages or end cap slots 31 and 35 are preferably located in the end cap 40 or 42 in an area between first end cap end 32 and opposing second end 34 of the end cap 40 or 42. In one aspect, the positioning passages or end cap slots 31 and 35 are substantially parallel to each other. The end cap 40 or 42 preferably has at least the same number of end cap slots 31 and 35 as the number of extending positioning teeth 30 which can align 37 with the end cap slots 31 and 35, so that the end cap 40 or 42 can be slideably inserted when the end cap 40 or 42 is moved onto the implant base section 15 and 25. In the aspect show in
The end cap 40 or 42 preferably has at least the same number of end cap slots 31 as the number of positioning teeth 30 which can align 37 as a single or a set of positioning teeth 30 so that the end cap 40 or 42 can be slideably inserted and positioned when the end cap 40 or 42 is positioned on the implant base section 15 and 25. This is the case since the positioning passages or end cap slots 31 accept entry of single or aligned 37 positioning teeth 30. For example, in the case shown in
In operation or use, the end cap slots 31 and 35 will engage and interlock with the plurality of corresponding and complementary positioning teeth 30 to form an end cap locking mechanism 50, shown in
The holding strength or force of the locking fit may be augmented or controlled by the addition or use of a coating substance between the end cap slots 31 and 35 and the positioning teeth 30, and in the exterior end cap slots 35 the selection and use of different tenon materials with different resilient physical properties to locking hold the positioning teeth 30. For example, a coating, such a silicone, may be used to for an increased friction fit between the end cap slots 31 and 35 and the positioning teeth 30. Those of skill in the art will recognize that other substances, friction control mechanism or physical materials may be used to augment or control holding strength or force between the end cap slots 31 & 35 and the positioning teeth 30. Also, those of skill in the art will recognize that instead of a friction fit, other types of interlocking fit may be used, e.g., an interference fit, press fit, snap fit, etc. Further, as previously discussed, the complementary positioning teeth 30 and interior positioning passages or end cap slots 31 in the locking mechanism 50 cooperatively interact to prevent movement of the end cap 40 or 42 relative to the first or second base section 15 or 25 in an axial direction along the implant axis 5. Since the tooth head 29 is wider and larger than the tooth base 28, an attempt to axially move or remove the end cap 40 or 42 will result in the end cap slot shoulder walls 27 butting up against the underside of the tooth head 29 which thereby prevents the axial movement, and axial removal, of the end cap 40 or 42 from the first or second base section 15 or 25.
The complementary positioning passages or end cap slots 31 and 35 and positioning teeth 30, when lockingly engaged, result in a locking engagement sufficient to hold the end cap 40 or 42 on the implant base plate 15 or 25 to permit a surgeon to pre-assemble the end cap 40 or 42 to an implant 10 for insertion into an intervertebral disc space 101. Those of skill in the art will recognize that other sizes, shapes and configuration may be used for the positioning passages 31 and 35 and positioning teeth 30 depending on medical procedure or clinical need, or surgeon need or selection, as long as they have a complementary configurations which permits sliding insertion and positioning, and locking engagement of the end cap slots 31 and 35 and the positioning teeth 30 when the end cap 40 is positioned on the implant base section 15 and 25.
The end cap 40 or 42 is preferably selectively positioned or adjusted on the implant base section 15 or 25 through variation in the approach direction and orientation XY of the positioning passages or end cap slots 31 and 35 to the implant base section 15 and 25. The approach direction XY of the positioning passages 31 and 35 is selectively adjustable relative to the implant body 20 and implant base section 15 or 25 about the longitudinal axis 5 of the implant body 20. The approach direction XY of the positioning passages or end cap slots 31 and 35 determines the position at which the end cap 40 will be placed at or located on the implant base section 15 and 25. The more approach directions XY available to the positioning passages or end cap slots 31 and 35, the greater the degree of choice and control a surgeon will have in placing the end cap 40 or 42 on the implant base section 15 and 25 at a desired or final position or orientation. This aspect advantageously provides a surgeon selective control of where the end cap angulation θ and the end cap vertex height H will be positioned on the implant base section 15 or 25. The ability to selectively position the end cap angulation θ permits a surgeon to determine where the end cap angulation θ and end cap height H will be applied or imparted to an adjacent vertebral body 100 or 105. Prior to insertion of the implant 10 into the intervertebral disc space 101, the surgeon can decide where the end cap angulation θ and the end cap vertex height H are desired or needed for a particular medical procedure or clinical application. The surgeon can then select the appropriate approach direction XY for the positioning passages or end cap slots 31 and 35 to take so that the end cap 40 or 42 can be slideably positioned on the implant base section 15 or 25 to impart the desired end cap angulation θ and end cap height H to an adjacent vertebral body 100 or 105.
An appropriate approach direction XY is selected for the positioning passages or end cap slots 31 and 35 in order to selectively position the end cap 40 on the implant base plate 15 or 25. There will be a plurality of possible or available approach directions XY. The end cap slots 31 and 35 can then be slideably positioned and inserted onto the positioning teeth 30 of the implant base plate 15 or 25 at the desired or needed approach direction XY. As an illustration,
The number of end cap slots 31 and 35 and corresponding sets of single or aligned positioning teeth 30 will impact the incremental degree of control, through the selectable end cap approach direction XY, that a surgeon will have in selecting the end cap angulation θ position between the implant 10 and the adjacent vertebral body 100 or 105. In one preferred aspect, shown in
A greater degree of control for incrementally advancing the end cap 40 or 42 about the implant base section 15 or 25, through appropriate selection of the approach direction XY, may be obtained by using a different number of end cap slots 31 and 35 and/or positioning teeth 30. For example, if the end caps 40 or 42 have the same four positioning passages or end cap slots 31 and 35 and the implant base sections 15 or 25 have eight positioning teeth 30. Then, the end cap 40 or 42 can be advanced, through appropriate selection of the approach direction XY, in single or multiple increments of forty-five degrees (45°) so as to position the end cap's angulation θ at different location points about the periphery of the adjacent vertebral body 100 or 105. In such a case, the end cap 40 or 42 can be selectively oriented to have a selective approach direction XY in order to position or reposition the end cap angulation θ point between the implant 10 and the adjacent vertebral body 100 or 105. The larger number of positioning teeth 30 coupled with the four positioning passages or end cap slots 31 and 35, in this case, provides a surgeon with the ability to position or reposition the end cap 40 or 42 in smaller discrete increments. The greater degree of control provides the surgeon with more precise control on where the end cap angulation θ will be positioned between the implant 10 and the adjacent vertebral body 100 or 105. In this manner, the selected angulation θ and end cap vertex height H can be imparted to an adjacent vertebral member 100 or 105 to thereby impart or drive angular orientation and height adjustment of the adjacent vertebral member 100 or 105 for correction or improved alignment, angulation, orientation, and stabilization of the spine or spinal anatomy.
Once the end cap 40 or 42 is preferably aligned and oriented, through selection of an appropriate or desired approach direction XY, the surgeon can insert and slideably move or force the end cap 40 or 42 onto the first and second base sections 15 and 25 so that the end cap 40 engages and locks onto the implant base plate 15 or 25, as shown in
In this aspect, the positioning teeth 130 comprise a tooth head 129 and a tooth base 128 with a tooth base cutout 137. In this tooth base 128 configuration, the tooth head 129 extends laterally past the tooth base 128 over the tooth base cutout 137, as shown in
The positioning passages 131 are preferably end cap slots complementarily shaped and configured to permit the positioning teeth 130 to enter and slideably travel therein. In one aspect, the positioning passages or end cap slots 131 have an elongated aperture configuration with slot shoulder wall 127 which will interact with the tooth base cutout 137 at the underside of the positioning teeth heads 129. The positioning passages or end cap slots 131 extend from a first end 132 of the end cap 140 across and towards an opposing second end of the end cap 140. The positioning passages or end cap slots 131 are complementarily sized to permit the end cap teeth 130 to enter and slideably travel within the positioning passages 131 as the end cap 140 is moved across the base sections 115. The complementary positioning teeth 130 and end cap slots 131 enable the end cap 140 to be slid onto the first base section 115, and interact and engage the complementary positioning passages 131 to form the end cap locking mechanism 150.
Further, as the end cap 140 slideably travels over and across the exterior surface 116 of the implant base section 115, the exterior positioning teeth 145 also enter and engage the exterior positioning passages or end cap slots 135, and thereafter slideably travel in the exterior end cap slots 135 between a locking tenon 136 and lateral wall 138. As the exterior positioning teeth 145 travel in the exterior end cap slots 135, the exterior positioning teeth 145 then encounter a tooth holding surface 139 which extends interiorly from the locking tenon 136. The exterior positioning teeth 145 will impart an outward force on the tooth holding surface 139 and the locking tenon 136. When the outward force overcomes the locking tenon's initial equilibrium position, the locking tenon 136 will deflect outwardly away from the initial equilibrium position. The locking tenon's 136 deflection permits the positioning tooth 145 to continue its sliding travel into the exterior end cap slot 135. When the exterior positioning teeth 145 slideably travels past the tooth holding surface 139, the locking tenon 136 will bias back towards its initial equilibrium position. When the exterior positioning teeth 145 reaches and abuts up against the positioning passage slot wall 133, the slot wall 133 will prevent further travel of the exterior positioning teeth 145 in the exterior end cap slot 135. At this position, the locking tenon 136 together with the tooth holding surface 139 and exterior positioning passage rear slot wall 133 lock the exterior positioning teeth 145 in the exterior end cap slot 135. The positioning teeth 145 will remain in the locked position until sufficient force is applied to overcome the locking tenon's holding force and permit slideable removal of the end cap 140.
In the locked position, the fit between the interlocking or engaging interior positioning teeth 130 and interior end cap slots 131, and exterior positioning teeth 145 and exterior end cap slots 135 is a friction fit sufficient to minimize or prevent movement between the positioning teeth 130 and 145 and end cap slots 131 and 135 once the end cap 140 is positioned at a desired end cap position on the first base section 115. Further, in this locking mechanism aspect 150, the locking tenon's 136 resilient or spring like property provides a holding force which strengthens the locking engagement between the exterior positioning teeth 145 and exterior end cap slots 135.
Additionally, the interior positioning teeth 130 and complementary interior positioning passages 131 cooperatively engage and interact to prevent movement or travel of the end cap 140 in an axial direction along an implant axis 106 relative to the implant base section 115. Since the tooth head 129 extends over and past the than the tooth base 128 at the tooth base cut out 128A, an attempt to move or remove the end cap 140 in an axial direction will result in the end cap slot shoulder walls 127 butting up against the underside of the tooth head 129 at the tooth base cut out 128A thereby preventing axial movement or removal of the end cap 140 from the first or implant base section 115.
The implants 10 and end caps 40, 42, and 140 may be implanted within a living patient for the treatment of various spinal disorders. The implants 10 and end caps 40, 42, and 140 may also be implanted in a non-living situation, such as within a cadaver, model, and the like. The non-living situation may be for one or more of testing, training, and demonstration purposes.
The end caps disclosed in this disclosure are preferably comprised of biocompatible materials substrates which can be used in combination with implants or devices configured to be inserted into an intervertebral space and contact against adjacent vertebral members. The biocompatible material substrate may include, among others, polyetheretherketone (PEEK) polymer material, homopolymers, co-polymers and oligomers of polyhydroxy acids, polyesters, polyorthoesters, polyanhydrides, polydioxanone, polydioxanediones, polyesteramides, polyaminoacids, polyamides, polycarbonates, polylactide, polyglycolide, tyrosine-derived polycarbonate, polyanhydride, polyorthoester, polyphosphazene, polyethylene, polyester, polyvinyl alcohol, polyacrylonitrile, polyamide, polytetrafluorethylene, poly-paraphenylene terephthalamide, polyetherketoneketone (PEKK); polyaryletherketones (PAEK), cellulose, carbon fiber reinforced composite, and mixtures thereof. The biocompatible material substrate may also be a metallic material and may include, among others, stainless steel, titanium, nitinol, platinum, tungsten, silver, palladium, cobalt chrome alloys, shape memory nitinol and mixtures thereof. The biocompatible material used can depend on the patient's need and physician requirements.
While embodiments of the invention have been illustrated and described in the present disclosure, the disclosure is to be considered as illustrative and not restrictive in character. The present invention may be carried out in other specific ways than those herein set forth without departing from the scope and essential characteristics of the invention. The present embodiments are, therefore, to be considered in all respects as illustrative and not restrictive, and all changes coming within the meaning and equivalency range of the appended claims are intended to be embraced therein.