초록 ▼

The present invention provides methods and devices for treating the annulus of an intervertebral disc. The methods and devices can employ an expandable treatment device which is deployed at least partially in the subannular space. Fixation devices and methods are also disclosed, which help to secure

The present invention provides methods and devices for treating the annulus of an intervertebral disc. The methods and devices can employ an expandable treatment device which is deployed at least partially in the subannular space. Fixation devices and methods are also disclosed, which help to secure the treatment device in place.

대표청구항 ▼

The invention claimed is: 1. A method of treating an aperture in an annulus fibrosus of an intervertebral disc, comprising: providing at least one delivery tool having a proximal portion and a distal portion, said distal portion configured to deliver at least one reparative device; providing a repa

The invention claimed is: 1. A method of treating an aperture in an annulus fibrosus of an intervertebral disc, comprising: providing at least one delivery tool having a proximal portion and a distal portion, said distal portion configured to deliver at least one reparative device; providing a reparative device, said reparative device comprising at least first and second anchor portions and a flexible connecting assembly connecting said anchor portions, said connecting assembly configured to be shortened and comprising a locking element, the first and second anchor portions being releasably coupled to the distal portion of the delivery tool; introducing the distal portion of the delivery tool with the reparative device proximate annular tissue to be repaired; delivering at least a portion of said at least one reparative device into, or through, a portion of the annulus, wherein, upon delivery, such that the first and second anchor portions reside within intervertebral disc tissue, including inserting the first anchor portion and at least a portion of the connecting assembly into or through an outer wall of the annulus fibrosus at a first insertion location proximate the aperture, inserting the second anchor portion and at least a portion of the connecting assembly into or through the outer wall of the annulus fibrosus at a second insertion location proximate the aperture, the second insertion location being separated from the first insertion location such that the aperture is located between the first and second insertion locations, and extending a portion of the connecting assembly across the aperture external to the outer wall of the annulus fibrosus; actuating said delivery tool, said actuating step causing the release of said reparative device from the delivery tool; shortening the connecting assembly disposed between the anchor portions so as to draw together, at least partially, annular tissue between the first and second anchor portions thereby at least partially drawing together annular tissue defining the aperture between the first and second insertion locations; securing said connecting assembly in a shortened configuration with a locking element; and, removing said delivery tool. 2. A method of claim 1, wherein said reparative device is comprised of one or more bands, filaments, lines, wires, tethers or sutures. 3. A method of claim 1, wherein said reparative device comprises biodegradable or bioabsorbable material. 4. A method of claim 1, wherein said reparative device comprises biocompatible material. 5. A method of claim 1, wherein said reparative device comprises material to facilitate regeneration of tissue. 6. A method of claim 5, wherein said material to facilitate regeneration of tissue comprises a growth factor. 7. A method of claim 1, wherein said reparative device comprises polymeric material. 8. A method of claim 1, wherein said anchor portion disposed within the intervertebral disc comprises a t-anchor or barb configuration. 9. A method of claim 1, wherein that the portion of said connecting assembly that is contiguous with said anchor portions is of a smaller girth than a portion of the connecting assembly disposed in between said anchor portions. 10. A method of claim 1, wherein said locking element of said connecting assembly comprises a retainer, clip, or knot. 11. A method of claim 10, wherein said knot is pre-tied. 12. A method of claim 1, wherein multiple reparative devices are used to treat an intervertebral disc. 13. A method of claim 1, wherein said reparative device is used in combination with a treatment device, said treatment device comprising mesh, scaffold, stent, patch, membrane, or tissue reinforcing materials, and wherein said treatment device is delivered to the intervertebral disc with a treatment device delivery tool. 14. A method of claim 13, wherein said treatment device comprises a retention element so as to secure the treatment device in a deployed configuration. 15. A method of claim 13, wherein said treatment device is configured to be attached by compression to a distal portion of the treatment device delivery tool, and capable of being released from the distal portion of the treatment device delivery tool upon relief of said compression. 16. A method of claim 13, wherein said treatment device comprises biodegradable or bioabsorbable material. 17. A method of claim 13, wherein said treatment device comprises biocompatible material. 18. A method of claim 13, wherein said treatment device comprises material to facilitate regeneration of tissue. 19. A method of claim 18, wherein said material to facilitate regeneration of tissue comprises a growth factor. 20. A method of claim 13, wherein said treatment device comprises polymeric material. 21. A method of treating an aperture in an annulus fibrosus of an intervertebral disc, comprising: providing a delivery tool including first and second needles each having a distal portion; providing a reparative device including first and second anchor portions and a connecting assembly connecting the anchor portions, the connecting assembly configured to be shortened and including a locking element, the first anchor portion being releasably coupled to the distal portion of the first needle, and the second anchor portion being releasably coupled to the distal portion of the second needle; inserting the distal portion of the first needle with the first anchor portion coupled thereto into or through an outer wall of the annulus at a first insertion location proximate the aperture in the annulus fibrosus; inserting the distal portion of the second needle with the second anchor portion coupled thereto into or through the outer wall of the annulus fibrosus at a second insertion location proximate the aperture in the annulus fibrosus, the second insertion location being separated from the first insertion location such that the aperture is located between the first and second insertion locations; extending a portion of the connecting assembly across the aperture external to the outer wall of the annulus fibrosus; causing or allowing the first anchor portion to be released from the first needle, and causing or allowing the second anchor portion to be released from the second needle, wherein, upon release, the first and second anchor portions reside within intervertebral disc tissue; shortening the connecting assembly disposed between anchor portions so as to draw together, at least partially, annular tissue between the first and second insertion locations thereby at least partially drawing together annular tissue defining the aperture between the first and second insertion locations; securing the connecting assembly in a shortened configuration with the locking element; and, removing the delivery tool.