Other products from "NUVASIVE, INC."
No Primary DI Version or Model Catalog Number Device Description Product Code Product Code Name Device Class Brand Name
1 00887517399779 6942044 CoRoent® XLR, 20x34x24 12° MAX Intervertebral fusion device with bone graft, lumbar 2 CoRoent
2 00887517399700 6941844 CoRoent® XLR, 18x34x24 12° MAX Intervertebral fusion device with bone graft, lumbar 2 CoRoent
3 00887517399335 6941644 CoRoent® XLR, 16x34x24 12° MAX Intervertebral fusion device with bone graft, lumbar 2 CoRoent
4 00887517398765 6941444 CoRoent® XLR, 14x34x24 12° MAX Intervertebral fusion device with bone graft, lumbar 2 CoRoent
5 00887517398499 6941244 CoRoent® XLR, 12x34x24 12° MAX Intervertebral fusion device with bone graft, lumbar 2 CoRoent
6 00887517398420 6941044 CoRoent® XLR, 10x34x24 12° MAX Intervertebral fusion device with bone graft, lumbar 2 CoRoent
7 00887517398055 6932088 CoRoent® XLR, 20x38x28 15° MAX Intervertebral fusion device with bone graft, lumbar 2 CoRoent
8 00887517397683 6931888 CoRoent® XLR, 18x38x28 15° MAX Intervertebral fusion device with bone graft, lumbar 2 CoRoent
9 00887517397256 6931688 CoRoent® XLR, 16x38x28 15° MAX Intervertebral fusion device with bone graft, lumbar 2 CoRoent
10 00887517396822 6931488 CoRoent® XLR, 14x38x28 15° MAX Intervertebral fusion device with bone graft, lumbar 2 CoRoent
11 00887517396457 6931288 CoRoent® XLR, 12x38x28 15° MAX Intervertebral fusion device with bone graft, lumbar 2 CoRoent
12 00887517395641 6922088 CoRoent® XLR, 20x38x28 8° MAX Intervertebral fusion device with bone graft, lumbar 2 CoRoent
13 00887517395634 6922044 CoRoent® XLR, 20x34x24 8° MAX Intervertebral fusion device with bone graft, lumbar 2 CoRoent
14 00887517395269 6921888 CoRoent® XLR, 18x38x28 8° MAX Intervertebral fusion device with bone graft, lumbar 2 CoRoent
15 00887517395252 6921844 CoRoent® XLR, 18x34x24 8° MAX Intervertebral fusion device with bone graft, lumbar 2 CoRoent
16 00887517394880 6921688 CoRoent® XLR, 16x38x28 8° MAX Intervertebral fusion device with bone graft, lumbar 2 CoRoent
17 00887517394873 6921660 CoRoent® XL Wide, 16x22x60mm Lordotic MAX Intervertebral fusion device with bone graft, lumbar 2 CoRoent
18 00887517394866 6921655 CoRoent® XL Wide, 16x22x55mm Lordotic MAX Intervertebral fusion device with bone graft, lumbar 2 CoRoent
19 00887517394859 6921650 CoRoent® XL Wide, 16x22x50mm Lordotic MAX Intervertebral fusion device with bone graft, lumbar 2 CoRoent
20 00887517394842 6921645 CoRoent® XL Wide, 16x22x45mm Lordotic MAX Intervertebral fusion device with bone graft, lumbar 2 CoRoent
21 00887517394835 6921644 CoRoent® XLR, 16x34x24 8° MAX Intervertebral fusion device with bone graft, lumbar 2 CoRoent
22 00887517394569 6921488 CoRoent® XLR, 14x38x28 8° MAX Intervertebral fusion device with bone graft, lumbar 2 CoRoent
23 00887517394552 6921460 CoRoent® XL Wide, 14x22x60mm Lordotic MAX Intervertebral fusion device with bone graft, lumbar 2 CoRoent
24 00887517394545 6921455 CoRoent® XL Wide, 14x22x55mm Lordotic MAX Intervertebral fusion device with bone graft, lumbar 2 CoRoent
25 00887517394538 6921450 CoRoent® XL Wide, 14x22x50mm Lordotic MAX Intervertebral fusion device with bone graft, lumbar 2 CoRoent
26 00887517394521 6921445 CoRoent® XL Wide, 14x22x45mm Lordotic MAX Intervertebral fusion device with bone graft, lumbar 2 CoRoent
27 00887517394514 6921444 CoRoent® XLR, 14x34x24 8° MAX Intervertebral fusion device with bone graft, lumbar 2 CoRoent
28 00887517394149 6921288 CoRoent® XLR, 12x38x28 8° MAX Intervertebral fusion device with bone graft, lumbar 2 CoRoent
29 00887517394132 6921260 CoRoent® XL Wide, 12x22x60mm Lordotic MAX Intervertebral fusion device with bone graft, lumbar 2 CoRoent
30 00887517394125 6921255 CoRoent® XL Wide, 12x22x55mm Lordotic MAX Intervertebral fusion device with bone graft, lumbar 2 CoRoent
31 00887517394118 6921250 CoRoent® XL Wide, 12x22x50mm Lordotic MAX Intervertebral fusion device with bone graft, lumbar 2 CoRoent
32 00887517394101 6921245 CoRoent® XL Wide, 12x22x45mm Lordotic MAX Intervertebral fusion device with bone graft, lumbar 2 CoRoent
33 00887517393791 6921244 CoRoent® XLR, 12x34x24 8° MAX Intervertebral fusion device with bone graft, lumbar 2 CoRoent
34 00887517393722 6921088 CoRoent® XLR, 10x38x28 8° MAX Intervertebral fusion device with bone graft, lumbar 2 CoRoent
35 00887517393715 6921060 CoRoent® XL Wide, 10x22x60mm Lordotic MAX Intervertebral fusion device with bone graft, lumbar 2 CoRoent
36 00887517393708 6921055 CoRoent® XL Wide, 10x22x55mm Lordotic MAX Intervertebral fusion device with bone graft, lumbar 2 CoRoent
37 00887517393395 6921050 CoRoent® XL Wide, 10x22x50mm Lordotic MAX Intervertebral fusion device with bone graft, lumbar 2 CoRoent
38 00887517393388 6921045 CoRoent® XL Wide, 10x22x45mm Lordotic MAX Intervertebral fusion device with bone graft, lumbar 2 CoRoent
39 00887517393371 6921044 CoRoent® XLR, 10x34x24 8° MAX Intervertebral fusion device with bone graft, lumbar 2 CoRoent
40 00887517393333 6920860 CoRoent® XL Wide, 8x22x60mm Lordotic MAX Intervertebral fusion device with bone graft, lumbar 2 CoRoent
41 00887517393326 6920855 CoRoent® XL Wide, 8x22x55mm Lordotic MAX Intervertebral fusion device with bone graft, lumbar 2 CoRoent
42 00887517393319 6920850 CoRoent® XL Wide, 8x22x50mm Lordotic MAX Intervertebral fusion device with bone graft, lumbar 2 CoRoent
43 00887517393302 6920845 CoRoent® XL Wide, 8x22x45mm Lordotic MAX Intervertebral fusion device with bone graft, lumbar 2 CoRoent
44 00887517392961 6916860 CoRoent® XL, 16x18x60mm MAX Intervertebral fusion device with bone graft, lumbar 2 CoRoent
45 00887517392954 6916855 CoRoent® XL, 16x18x55mm MAX Intervertebral fusion device with bone graft, lumbar 2 CoRoent
46 00887517392947 6916850 CoRoent® XL, 16x18x50mm MAX Intervertebral fusion device with bone graft, lumbar 2 CoRoent
47 00887517392930 6916845 CoRoent® XL, 16x18x45mm MAX Intervertebral fusion device with bone graft, lumbar 2 CoRoent
48 00887517392923 6916840 CoRoent® XL, 16x18x40mm MAX Intervertebral fusion device with bone graft, lumbar 2 CoRoent
49 00887517392916 6916260 CoRoent® XL Wide, 16x22x60mm MAX Intervertebral fusion device with bone graft, lumbar 2 CoRoent
50 00887517392909 6916255 CoRoent® XL Wide, 16x22x55mm MAX Intervertebral fusion device with bone graft, lumbar 2 CoRoent
Other products with the same Product Code "ODP"
No Primary DI Version or Model Catalog Number Device Description Brand Name Organization Name
1 00813210020856 CIC2-10-12-00 The Wenzel Spine VariLift-C Cervical Interbody Fusion Device System consists of The Wenzel Spine VariLift-C Cervical Interbody Fusion Device System consists of a self-tapping, expandable device with an interior expansion plate, and is grooved and fluted with large graft windows positioned between each of its four quadrants that provide bony contact with the endplates. VariLift-C may be used with or without supplemental fixation. VariLift-C is indicated for use in skeletally mature patients with degenerative disc disease (DDD) of the cervical spine with accompanying radicular symptoms at one disc level. DDD is defined as discogenic pain with degeneration of the disc confirmed by patient history and radiographic studies. Patients should have at least six weeks of non-operative treatment prior to treatment with VariLift-C. These DDD patients may have up to Grade 1 spondylolisthesis or retrolisthesis at the involved level. The VariLift-C is used to facilitate intervertebral body fusion in the cervical spine and is placed in a unilateral or a bilateral fashion via an anterior approach at the C3 to C7 disc levels using autograft bone. VariLift-C WENZEL SPINE, INC.
2 00813210020849 CIC2-09-12-00 The Wenzel Spine VariLift-C Cervical Interbody Fusion Device System consists of The Wenzel Spine VariLift-C Cervical Interbody Fusion Device System consists of a self-tapping, expandable device with an interior expansion plate, and is grooved and fluted with large graft windows positioned between each of its four quadrants that provide bony contact with the endplates. VariLift-C may be used with or without supplemental fixation. VariLift-C is indicated for use in skeletally mature patients with degenerative disc disease (DDD) of the cervical spine with accompanying radicular symptoms at one disc level. DDD is defined as discogenic pain with degeneration of the disc confirmed by patient history and radiographic studies. Patients should have at least six weeks of non-operative treatment prior to treatment with VariLift-C. These DDD patients may have up to Grade 1 spondylolisthesis or retrolisthesis at the involved level. The VariLift-C is used to facilitate intervertebral body fusion in the cervical spine and is placed in a unilateral or a bilateral fashion via an anterior approach at the C3 to C7 disc levels using autograft bone. VariLift-C WENZEL SPINE, INC.
3 00813210020832 CIC2-08-12-00 The Wenzel Spine VariLift-C Cervical Interbody Fusion Device System consists of The Wenzel Spine VariLift-C Cervical Interbody Fusion Device System consists of a self-tapping, expandable device with an interior expansion plate, and is grooved and fluted with large graft windows positioned between each of its four quadrants that provide bony contact with the endplates. VariLift-C may be used with or without supplemental fixation. VariLift-C is indicated for use in skeletally mature patients with degenerative disc disease (DDD) of the cervical spine with accompanying radicular symptoms at one disc level. DDD is defined as discogenic pain with degeneration of the disc confirmed by patient history and radiographic studies. Patients should have at least six weeks of non-operative treatment prior to treatment with VariLift-C. These DDD patients may have up to Grade 1 spondylolisthesis or retrolisthesis at the involved level. The VariLift-C is used to facilitate intervertebral body fusion in the cervical spine and is placed in a unilateral or a bilateral fashion via an anterior approach at the C3 to C7 disc levels using autograft bone. VariLift-C WENZEL SPINE, INC.
4 00813210020788 CIC2-A743 Expander VariLift-C WENZEL SPINE, INC.
5 00813210020771 CIC2-A742 Retainer VariLift-C WENZEL SPINE, INC.
6 00813210020764 CIC2-A741 Inserter VariLift-C WENZEL SPINE, INC.
7 00813210020719 CIC1-A743-C01 Expansion Wrench, T-Handle VariLift-C WENZEL SPINE, INC.
8 00813210020702 CIC1-A741-C01 Insertion Wrench, T-Handle VariLift-C WENZEL SPINE, INC.
9 00813210020252 CIC1-A747 Removal Screwdriver VariLift-C WENZEL SPINE, INC.
10 00813210020221 CIC1-A743 Expansion Wrench VariLift-C WENZEL SPINE, INC.
11 00813210020214 CIC1-A742 Locking Wrench VariLift-C WENZEL SPINE, INC.
12 00813210020207 CIC1-A741 Insertion Wrench VariLift-C WENZEL SPINE, INC.
13 00813210020061 CIC1-9.0-12-00 The Wenzel Spine VariLift-C Cervical Interbody Fusion Device System consists of The Wenzel Spine VariLift-C Cervical Interbody Fusion Device System consists of a self-tapping, expandable device with an interior expansion plate, and is grooved and fluted with large graft windows positioned between each of its four quadrants that provide bony contact with the endplates. VariLift-C may be used with or without supplemental fixation. VariLift-C is indicated for use in skeletally mature patients with degenerative disc disease (DDD) of the cervical spine with accompanying radicular symptoms at one disc level. DDD is defined as discogenic pain with degeneration of the disc confirmed by patient history and radiographic studies. Patients should have at least six weeks of non-operative treatment prior to treatment with VariLift-C. These DDD patients may have up to Grade 1 spondylolisthesis or retrolisthesis at the involved level. The VariLift-C is used to facilitate intervertebral body fusion in the cervical spine and is placed in a unilateral or a bilateral fashion via an anterior approach at the C3 to C7 disc levels using autograft bone. VariLift-C WENZEL SPINE, INC.
14 00813210020054 CIC1-7.5-12-00 The Wenzel Spine VariLift-C Cervical Interbody Fusion Device System consists of The Wenzel Spine VariLift-C Cervical Interbody Fusion Device System consists of a self-tapping, expandable device with an interior expansion plate, and is grooved and fluted with large graft windows positioned between each of its four quadrants that provide bony contact with the endplates. VariLift-C may be used with or without supplemental fixation. VariLift-C is indicated for use in skeletally mature patients with degenerative disc disease (DDD) of the cervical spine with accompanying radicular symptoms at one disc level. DDD is defined as discogenic pain with degeneration of the disc confirmed by patient history and radiographic studies. Patients should have at least six weeks of non-operative treatment prior to treatment with VariLift-C. These DDD patients may have up to Grade 1 spondylolisthesis or retrolisthesis at the involved level. The VariLift-C is used to facilitate intervertebral body fusion in the cervical spine and is placed in a unilateral or a bilateral fashion via an anterior approach at the C3 to C7 disc levels using autograft bone. VariLift-C WENZEL SPINE, INC.
15 00813210020047 CIC1-9.0-12-BP The Wenzel Spine VariLift-C Cervical Interbody Fusion Device System consists of The Wenzel Spine VariLift-C Cervical Interbody Fusion Device System consists of a self-tapping, expandable device with an interior expansion plate, and is grooved and fluted with large graft windows positioned between each of its four quadrants that provide bony contact with the endplates. VariLift-C may be used with or without supplemental fixation. VariLift-C is indicated for use in skeletally mature patients with degenerative disc disease (DDD) of the cervical spine with accompanying radicular symptoms at one disc level. DDD is defined as discogenic pain with degeneration of the disc confirmed by patient history and radiographic studies. Patients should have at least six weeks of non-operative treatment prior to treatment with VariLift-C. These DDD patients may have up to Grade 1 spondylolisthesis or retrolisthesis at the involved level. The VariLift-C is used to facilitate intervertebral body fusion in the cervical spine and is placed in a unilateral or a bilateral fashion via an anterior approach at the C3 to C7 disc levels using autograft bone. VariLift-C WENZEL SPINE, INC.
16 00813210020030 CIC1-7.5-12-BP The Wenzel Spine VariLift-C Cervical Interbody Fusion Device System consists of The Wenzel Spine VariLift-C Cervical Interbody Fusion Device System consists of a self-tapping, expandable device with an interior expansion plate, and is grooved and fluted with large graft windows positioned between each of its four quadrants that provide bony contact with the endplates. VariLift-C may be used with or without supplemental fixation. VariLift-C is indicated for use in skeletally mature patients with degenerative disc disease (DDD) of the cervical spine with accompanying radicular symptoms at one disc level. DDD is defined as discogenic pain with degeneration of the disc confirmed by patient history and radiographic studies. Patients should have at least six weeks of non-operative treatment prior to treatment with VariLift-C. These DDD patients may have up to Grade 1 spondylolisthesis or retrolisthesis at the involved level. The VariLift-C is used to facilitate intervertebral body fusion in the cervical spine and is placed in a unilateral or a bilateral fashion via an anterior approach at the C3 to C7 disc levels using autograft bone. VariLift-C WENZEL SPINE, INC.
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