Interspinous vertebral and lumbosacral stabilization devices and methods of use
View Patent ↗Implantable devices are provided for stabilizing adjacent vertebrae and the lumbosacral region of a patient. The devices can comprise an interspinous flexible spacer body having a substantially U-shape comprising a superior section, inferior section, and a midsection extending therebetween. The superior and/or inferior sections can include a pair of lateral walls configured to engage a spinous process of a vertebra. Fixation caps can be provided for securing a spinous process of a vertebra to the flexible spacer body. To secure the flexible spacer body between the lumbar vertebra and an adjacent vertebra, an anchor assembly is provided. Also provided are methods of using the implantable devices to stabilize a patient's spine.
1. A lumbosacral interspinous stabilization device, comprising:
an inferior section, a superior section extending substantially parallel to the inferior section, and a flexible U-shaped midsection connecting the inferior section to the superior section, the inferior section, superior section and midsection together forming a substantially U-shaped spacer body configured to extend into the interspinous space, and further including a pair of lateral walls extending from the superior section for engaging a spinous process of a lumbar vertebra, and a plurality of projections extending from the inferior section, the plurality of projections including a pair of endplates configured to grip therebetween a portion of a sacrum, each endplate including at least one screw hole for receiving a bone screw, the bone screw being configured to extend through the at least one screw hole of one endplate, through bone tissue, and out the at least one screw hole of the other endplate.
2. The device of claim 1 , wherein the lumbar vertebra is a fifth lumbar vertebra (L5).
3. The device of claim 1 , wherein the flexibility of the body varies along its length.
4. The device of claim 1 , wherein the thickness of the body varies along its length.
5. The device of claim 1 , wherein the width of the body varies along its length.
6. The device of claim 1 , wherein the lateral walls extend substantially parallel to one another prior to implantation.
7. The device of claim 1 , wherein the lateral walls extend away from one another prior to implantation.
8. The device of claim 1 , wherein the lateral walls are configured to be movable towards one another after implantation.
9. The device of claim 1 , wherein the lateral walls are malleable.
10. The device of claim 1 , wherein each lateral wall contains a through hole.
11. The device of claim 10 , further comprising a flexible fixation element configured to be tied around the through holes and around the spinous process.
12. The device of claim 11 , wherein the flexible fixation element is a synthetic or natural material.
13. The device of claim 12 , wherein the synthetic or natural material is selected from the group consisting of ligament, tendon, fascia, muscle, suture material, fabric, mesh, and webbing.
14. The device of claim 10 , further including a fastener for placement between the through holes of the lateral walls.
15. The device of claim 14 , further including a cap for placement over a distal portion of the fastener.
16. The device of claim 14 , further including a washer for placement over a distal portion of the fastener.
17. The device of claim 1 , wherein the device includes surface features for enhanced fixation to bone tissue.
18. The device of claim 17 , wherein the surface features are selected from the group consisting of teeth, barbs, beads, and surface roughening.
19. The device of claim 1 , wherein the device further includes a biologically active material to promote tissue growth after implantation.
20. The device of claim 19 , wherein the biologically active material is contained in a coating on the device.
21. The device of claim 19 , wherein the device is porous and the biologically active material is contained in the pores of the device.
22. The device of claim 1 , wherein the device is comprised of a biocompatible metal or polymer.
23. The device of claim 22 , wherein the biocompatible metal or polymer is selected from the group consisting of titanium, titanium alloy, stainless steel, cobalt chrome, ceramics, ultra high molecular weight polyethylene and polyetheretherketone.