Other products from "CAPTIVA SPINE, INC."
No Primary DI Version or Model Catalog Number Device Description Product Code Product Code Name Device Class Brand Name
1 M739PS32130 PS3213 MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 TLIF Straight, 32 x 13mm
2 M739PI0703 PI-0703 HTF Curette 1 Tear Drop Curette CR
3 M739PL36090 PL3609 MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 TLIF Curved-L, 36 x 9mm
4 M739245530300 2455-3030 MNH,MNI Orthosis, Spondylolisthesis Spinal Fixation,Orthosis, Spinal Pedicle Fixation 2 PivoRod MIS Curved Rod 5.5 x 30
5 M739241249550 2412-4955 MNH,MNI Orthosis, Spondylolisthesis Spinal Fixation,Orthosis, Spinal Pedicle Fixation 2 Polyaxial Screw, 4.9 x 55
6 M7391931930000 19319-3000 Curved Tamp MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 TirboLOX-L Lumbar IBFD
7 M739133400014 13340-0014 LXH Orthopedic Manual Surgical Instrument 1 14mm Drill Bit Spade Tip
8 M7391844000400 18440-0040 OJH Orthopedic Tray 1 Modular Tray Component
9 M739153003007 15300-3007 LXH Orthopedic Manual Surgical Instrument 1 SG-Screwdriver
10 M739134990104 13499-0104 LXH Orthopedic Manual Surgical Instrument 1 RLC Bone Awl Sleeve
11 M739PI0708 PI-0708 LXH Orthopedic Manual Surgical Instrument 1 Rasp Bilateral Angled
12 M739PI0706 PI-0706 HTF Curette 1 Cup Curette with Teeth CR
13 M739ST06016 ST06016 Variable Self-Drilling Screws, 4 mm x 16mm KWQ Appliance, Fixation, Spinal Intervertebral Body 2 Variable Self-Drilling Screws, 4 mm x 16mm
14 M739PS30160 PS3016 MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 TLIF Straight, 30 x 16mm
15 M739PS3016 PS3016 TLIF Straight, 30 x 16mm MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 TLIF Straight, 30 x 16mm
16 M739PS28110 PS2811 MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 TLIF Straight, 28 x 11mm
17 M739PS2811 PS2811 TLIF Straight, 28 x 11mm MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 TLIF Straight, 28 x 11mm
18 M739PP36160 PP3616 MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 TLIF Curved-P, 36 x 16mm
19 M739PP3616 PP3616 TLIF Curved-P, 36 x 16mm MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 TLIF Curved-P, 36 x 16mm
20 M739PP34080 PP3408 MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 TLIF Curved-P, 34 x 8mm
21 M739PP3408 PP3408 TLIF Curved-P, 34 x 8mm MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 TLIF Curved-P, 34 x 8mm
22 M739PP32150 PP3215 MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 TLIF Curved-P, 32 x 15mm
23 M739PP3215 PP3215 TLIF Curved-P, 32 x 15mm MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 TLIF Curved-P, 32 x 15mm
24 M739PP30110 PP3011 MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 TLIF Curved-P, 30 x 11mm
25 M739PP3011 PP3011 TLIF Curved-P, 30 x 11mm MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 TLIF Curved-P, 30 x 11mm
26 M739PL36160 PL3616 MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 TLIF Curved-L, 36 x 16mm
27 M739PL3616 PL3616 TLIF Curved-L, 36 x 16mm MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 TLIF Curved-L, 36 x 16mm
28 M739PL32110 PL3211 MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 TLIF Curved-L, 32 x 11mm
29 M739PL3211 PL3211 TLIF Curved-L, 32 x 11mm MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 TLIF Curved-L, 32 x 11mm
30 M739PL32080 PL3208 MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 TLIF Curved-L, 32 x 8mm
31 M739PL3208 PL3208 TLIF Curved-L, 32 x 8mm MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 TLIF Curved-L, 32 x 8mm
32 M739PI0611 PI-0611 LXH Orthopedic Manual Surgical Instrument 1 Trial CVD 30 x 11mm
33 M739PI0608 PI-0608 LXH Orthopedic Manual Surgical Instrument 1 Trial CVD 30 x 8mm
34 M739PI01500 PI-0150 LXH Orthopedic Manual Surgical Instrument 1 Pivo Inserter (Ti)
35 M739FPT32110 FPT3211 LXH Orthopedic Manual Surgical Instrument 1 Convex Trial 32 x 11mm
36 M739FPT30140 FPT3014 LXH Orthopedic Manual Surgical Instrument 1 Convex Trial 30 x 14mm
37 M739FPT2514 FPT2514 Trial 14mm LXH Orthopedic Manual Surgical Instrument 1 Trial 14mm
38 M739FPT2513 FPT2513 Trial 13mm LXH Orthopedic Manual Surgical Instrument 1 Trial 13mm
39 M739FPT25110 FPT2511 LXH Orthopedic Manual Surgical Instrument 1 Convex Trial 25 x 11mm
40 M739FPT2508 FPT2508 Trial 8mm LXH Orthopedic Manual Surgical Instrument 1 Trial 8mm
41 M739FPT2507 FPT2507 Trial 7mm LXH Orthopedic Manual Surgical Instrument 1 Trial 7mm
42 M739FPL3013 FPL3013 Lordotic Cage, 30 x 13mm MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 Lordotic Cage, 30 x 13mm
43 M739FPL3009 FPL3009 Lordotic Cage, 30 x 9mm MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 Lordotic Cage, 30 x 9mm
44 M739FPL3007 FPL3007 Lordotic Cage, 30 x 7mm MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 Lordotic Cage, 30 x 7mm
45 M739FPL2813 FPL2813 Lordotic Cage, 28 x 13mm MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 Lordotic Cage, 28 x 13mm
46 M739FPL2812 FPL2812 Lordotic Cage, 28 x 12mm MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 Lordotic Cage, 28 x 12mm
47 M739FPL25090 FPL2509 Lordotic Cage, 25 x 9mm MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 Lordotic Cage, 25 x 9mm
48 M739FPL2509 FPL2509 Lordotic Cage, 25 x 9mm MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 Lordotic Cage, 25 x 9mm
49 M739FPL25080 FPL2508 Lordotic Cage, 25 x 8mm MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 Lordotic Cage, 25 x 8mm
50 M739FPL2508 FPL2508 Lordotic Cage, 25 x 8mm MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 Lordotic Cage, 25 x 8mm
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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