Bioactive spinal implants and method of manufacture thereof
A bioactive spinal implant used in cervical fusion, Anterior Lumbar Interbody Fusion (ALIF), Posterior Lumbar Interbody Fusion (PLIF), and Transforaminal Interbody Fusion (TLIF), having properties and geometries that enhance bone contact, stability, and fusion between adjacent vertebral bodies.
1. A spinal implant system comprising:
a body comprising:
an anterior side, a posterior side opposing the anterior side, and a pair of opposing side walls, the anterior side, the posterior side, and side walls joining at points that generally define, in transverse cross section, a trapezoid said sides being generally outwardly curved;
a top surface and a bottom surface, each of the top and bottom surfaces including plural projections for enhancing interaction with a synthetic or natural vertebral body; and
a handling feature comprising a pair of elongated side recesses and a front recess, the handling feature facilitating handling and insertion of the spinal implant into an intervertebral space, wherein the elongated recesses each comprise an opening; and
a manipulator comprising a first arm and a second arm, the first and second arms being engageable with the elongated side recesses.
2. The spinal implant system of claim 1 wherein the generally outwardly curved sides are convex as viewed from outside said spinal implant.
3. The spinal implant system of claim 1 wherein the body forms a lordotic angle of about −20 degrees to about +20 degrees.
4. The spinal implant system of claim 1 wherein the height of the anterior side is greater than a height of the posterior side.
5. The spinal implant system of claim 1 wherein the body substantially forms a trapezoidal shape in longitudinal cross-section.
6. The spinal implant system of claim 1 wherein the projections are substantially uniform, upwardly protruding ribs.
7. The spinal implant system of claim 1 wherein the projections are randomly disposed.
8. The spinal implant system of claim 1 , wherein the first arm includes a first projection and the second arm includes a second projection, the first and second projections being configured for insertion into a respective one of the openings of the elongated recesses.
9. A spinal implant system comprising:
a body comprising a bioactive substance, further comprising:
sides that are generally outwardly curved in transverse cross-section;
a top surface and a bottom surface, both surfaces coupled with the sides, each one of the top surface and the bottom surface forming plural projections for enhancing interaction with a synthetic or natural vertebral body;
a major recess formed in the body in communication with at least one of the top surface and the bottom surface; and
a handling feature comprising a pair of elongated side recesses and a front recess, the handling feature facilitating handling and insertion of the spinal implant into an intervertebral space, wherein the elongated recesses each comprise an opening; and
a manipulator comprising a first arm and a second arm, the first and second arms being engageable with the elongated side recesses.
10. The spinal implant system of claim 9 wherein the body forms a lordotic angle of about −20 degrees to about +20 degrees.
11. The spinal implant system of claim 9 wherein the height of the anterior side is greater than the height of the posterior side.
12. The spinal implant system of claim 9 wherein the body substantially forms a trapezoidal shape in longitudinal cross-section.
13. The spinal implant system of claim 9 wherein the projections are substantially uniform, upwardly protruding ribs.
14. The spinal implant system of claim 9 , wherein the first arm includes a first projection and the second arm includes a second projection, the first and second projections being configured for insertion into a respective one of the openings of the elongated recesses.
15. A spinal implant system comprising:
a body comprising a bioactive substance, further comprising:
an anterior side, a posterior side opposing the anterior side, and a pair of opposing sidewalls, said sidewalls being generally outwardly curved;
a top surface and a bottom surface, both surfaces coupled with the sides, each one of the top surface and the bottom surface forming plural projections for enhancing interaction with a synthetic or natural vertebral body;
at least one major recess formed in the body in communication with at least one of the top surface and the bottom surface;
a handling feature comprising recesses in the top and bottom surfaces in communication with the anterior and posterior sides and at least one recess in the anterior or sidewalls for receiving an impaction tool, the handling feature facilitating handling and insertion of the spinal implant into an intervertebral space; and
a fastening feature comprising a first through-aperture angled through the anterior side, such that a fastener inserted into the first through-aperture is directed into a first synthetic or natural vertebral body.
16. The spinal implant system of claim 15 wherein the anterior and posterior sides are parallel.
17. The spinal implant system of claim 15 wherein the anterior and posterior sides are generally outwardly curved.
18. The spinal implant system of claim 15 wherein the lordotic angle ranges from about −20 degrees to about +20 degrees.
19. The spinal implant system of claim 15 wherein the height of the anterior side is greater than a height of the posterior side.
20. The spinal implant system of claim 15 wherein the major recess forms a longitudinal through-aperture.
21. The spinal implant system of claim 15 , wherein the fastening feature further comprises a second through-aperture angled through the anterior side, such that a fastener inserted into the second through-aperture is directed into a second synthetic or natural vertebral body.
22. The spinal implant system of claim 15 , wherein the at least one recess in the anterior or sidewalls has a geometry that matches a geometry of a portion of the impaction tool, such that upon engagement of the portion of the impaction tool with the at least one recess, the implant is rotationally fixed relative to the impaction tool.