초록 ▼

A system and method is provided for maintaining a proper intervertebral disc height during the replacement or augmentation of the spinal disc. In one embodiment, a cannulated distractor is used to distract the adjacent vertebrae and maintain a proper disc space height. The cannulated distractor is

A system and method is provided for maintaining a proper intervertebral disc height during the replacement or augmentation of the spinal disc. In one embodiment, a cannulated distractor is used to distract the adjacent vertebrae and maintain a proper disc space height. The cannulated distractor is fluidly connected to a source of fluent material for injection into the disc space. The distraction includes a distraction tip resident within the disc space that includes a central lumen and a number of openings communicating with the lumen to dispense the fluent material within the disc space.

대표청구항 ▼

What is claimed is: 1. A kit of parts for sealably introducing fluent material directly into the disc space having a height between opposed vertebrae through an opening extending through the annulus fibrosis of said disc for replacing nucleus pulposus, comprising: a tube having a passageway for the

What is claimed is: 1. A kit of parts for sealably introducing fluent material directly into the disc space having a height between opposed vertebrae through an opening extending through the annulus fibrosis of said disc for replacing nucleus pulposus, comprising: a tube having a passageway for the flow of fluent material therethrough and an extent adapted to be received in the opening of said annulus fibrosis, said tube having a seal adapted to engage said annulus fibrosis adjacent said opening and to form a fluid-tight seal therewith, wherein said tube extent is defined by a distal tip of said tube, said distal tip having a dimension greater than the height of said disc space that is sized and configured to provide distraction of opposed vertebrae communicating with said disc space; and a quantity of curable fluent material adapted to be introduced in a fluid state into said disc space through the passageway of said tube, said material upon curing having properties substitutive of the nucleus pulposus. 2. The kit of parts according to claim 1, wherein said seal is integral with said tube. 3. The kit of parts according to claim 1, wherein said seal is a separate component mounted on said tube. 4. The kit of parts according to claim 1, wherein said fluent material is a curable biomaterial selected from the group of nucleus pulposus substitutes consisting of hyaluronic acid, fibrin glue, alginates, elastin copolymers and collagen gels. 5. The kit of parts according to claim 1, wherein said distal tip comprises at least one orifice communicating with said passageway to provide an exit path for said fluent material into said disc space. 6. The kit of parts according to claim 1, wherein said distal tip is removable from said tube. 7. The kit of parts according to claim 6, wherein there are a plurality of removable distal tips, each being of different size. 8. The kit of parts according to claim 6, wherein said distal tip is formed of bioresorbable material. 9. The kit of parts according to claim 1, further including a syringe adapted to inject said fluent material into the passageway of said tube. 10. The kit of parts of claim 1, wherein said seal is adapted to reside within said opening of said annulus fibrosis. 11. The kit of parts according to claim 1, further including an injector adapted to be coupled to said tube for injecting said fluent material into said tube under pressure. 12. The kit of parts according to claim 11, wherein said injector includes a syringe. 13. The kit of parts according to claim 11, wherein said injector includes a pump. 14. The kit of parts according to claim 11, wherein said injector includes a mixing chamber.