Other products from "WENZEL SPINE, INC."
No Primary DI Version or Model Catalog Number Device Description Product Code Product Code Name Device Class Brand Name
1 00813210022300 800-0235 Polyaxial Plate Inserter KWP Appliance, Fixation, Spinal Interlaminal 2 primaLOK SP
2 00813210022294 800-0233 Post Plate Inserter KWP Appliance, Fixation, Spinal Interlaminal 2 primaLOK SP
3 00813210022096 800-1206 EMG Cannula LXH Orthopedic Manual Surgical Instrument 1 primaLOK FF
4 00813210022157 800-1221 3mm Cannulated Power Drill LXH Orthopedic Manual Surgical Instrument 1 primaLOK FF
5 00813210022133 800-1215 Ratcheting Driver Handle LXH Orthopedic Manual Surgical Instrument 1 primaLOK FF
6 00813210022126 800-1210 Cannula Inserter LXH Orthopedic Manual Surgical Instrument 1 primaLOK FF
7 00813210022119 800-1208 Single Bevel Access Needle (sterile, single use) LXH Orthopedic Manual Surgical Instrument 1 primaLOK FF
8 00813210022102 800-1207 Access Needle (sterile, single use) LXH Orthopedic Manual Surgical Instrument 1 primaLOK FF
9 00813210022089 800-1205 Standard Cannula LXH Orthopedic Manual Surgical Instrument 1 primaLOK FF
10 00813210022072 800-1204 Guide Wire Stiffener LXH Orthopedic Manual Surgical Instrument 1 primaLOK FF
11 00813210022065 800-1202 Cannulated Tap LXH Orthopedic Manual Surgical Instrument 1 primaLOK FF
12 00813210022041 800-1200 Guide Wire (single use, disposable) LXH Orthopedic Manual Surgical Instrument 1 primaLOK FF
13 00813210022034 800-1213 Threaded Implant Holder Shaft - Solid MRW System, Facet Screw Spinal Device U primaLOK FF
14 00813210022027 800-1212 Threaded Implant Holder Shaft - Cannulated MRW System, Facet Screw Spinal Device U primaLOK FF
15 00813210022010 800-1211 Implant Driver MRW System, Facet Screw Spinal Device U primaLOK FF
16 00813210022003 800-1203 Removal Driver MRW System, Facet Screw Spinal Device U primaLOK FF
17 00813210021990 800-1145-00 primaLOK FF 45mm Implant Assembly, Sterile primaLOK FF 45mm Implant Assembly, Sterile The Wenzel Spine primaLOK FF Facet Fixation System is intended to stabilize the spine as an aid to fusion through bilateral immobilization of the facet joints. It is intended for use with or without bone graft, at a single or multiple levels from L1 to S1 inclusive. It is indicated for the posterior surgical treatment of any or all of the following: degenerative disc disease (DDD) as defined by back pain of discogenic origin with degeneration of the facets with instability, trauma (i.e., fracture or dislocation), spondylolisthesis, spondylolysis, and pseudoarthrosis and failed fusions which are symptomatic or which may cause secondary instability or deformity. For transfacet fixation, the screws are inserted through the inferior articular process across the facet joint and into the pedicle. For translaminar facet fixation, the screws are inserted through the lateral aspect of the spinous process, through the lamina, through the inferior articular process, across the facet joint and into the pedicle. MRW System, Facet Screw Spinal Device U primaLOK FF
18 00813210021983 800-1140-00 primaLOK FF 40mm Implant Assembly, Sterile primaLOK FF 40mm Implant Assembly, Sterile The Wenzel Spine primaLOK FF Facet Fixation System is intended to stabilize the spine as an aid to fusion through bilateral immobilization of the facet joints. It is intended for use with or without bone graft, at a single or multiple levels from L1 to S1 inclusive. It is indicated for the posterior surgical treatment of any or all of the following: degenerative disc disease (DDD) as defined by back pain of discogenic origin with degeneration of the facets with instability, trauma (i.e., fracture or dislocation), spondylolisthesis, spondylolysis, and pseudoarthrosis and failed fusions which are symptomatic or which may cause secondary instability or deformity. For transfacet fixation, the screws are inserted through the inferior articular process across the facet joint and into the pedicle. For translaminar facet fixation, the screws are inserted through the lateral aspect of the spinous process, through the lamina, through the inferior articular process, across the facet joint and into the pedicle. MRW System, Facet Screw Spinal Device U primaLOK FF
19 00813210021976 800-1135-00 primaLOK FF 35mm Implant Assembly, Sterile primaLOK FF 35mm Implant Assembly, Sterile The Wenzel Spine primaLOK FF Facet Fixation System is intended to stabilize the spine as an aid to fusion through bilateral immobilization of the facet joints. It is intended for use with or without bone graft, at a single or multiple levels from L1 to S1 inclusive. It is indicated for the posterior surgical treatment of any or all of the following: degenerative disc disease (DDD) as defined by back pain of discogenic origin with degeneration of the facets with instability, trauma (i.e., fracture or dislocation), spondylolisthesis, spondylolysis, and pseudoarthrosis and failed fusions which are symptomatic or which may cause secondary instability or deformity. For transfacet fixation, the screws are inserted through the inferior articular process across the facet joint and into the pedicle. For translaminar facet fixation, the screws are inserted through the lateral aspect of the spinous process, through the lamina, through the inferior articular process, across the facet joint and into the pedicle. MRW System, Facet Screw Spinal Device U primaLOK FF
20 00813210021969 800-1130-00 primaLOK FF 30mm Implant Assembly, Sterile primaLOK FF 30mm Implant Assembly, Sterile The Wenzel Spine primaLOK FF Facet Fixation System is intended to stabilize the spine as an aid to fusion through bilateral immobilization of the facet joints. It is intended for use with or without bone graft, at a single or multiple levels from L1 to S1 inclusive. It is indicated for the posterior surgical treatment of any or all of the following: degenerative disc disease (DDD) as defined by back pain of discogenic origin with degeneration of the facets with instability, trauma (i.e., fracture or dislocation), spondylolisthesis, spondylolysis, and pseudoarthrosis and failed fusions which are symptomatic or which may cause secondary instability or deformity. For transfacet fixation, the screws are inserted through the inferior articular process across the facet joint and into the pedicle. For translaminar facet fixation, the screws are inserted through the lateral aspect of the spinous process, through the lamina, through the inferior articular process, across the facet joint and into the pedicle. MRW System, Facet Screw Spinal Device U primaLOK FF
21 00813210021952 800-1125-00 primaLOK FF 25mm Implant Assembly, Sterile primaLOK FF 25mm Implant Assembly, Sterile The Wenzel Spine primaLOK FF Facet Fixation System is intended to stabilize the spine as an aid to fusion through bilateral immobilization of the facet joints. It is intended for use with or without bone graft, at a single or multiple levels from L1 to S1 inclusive. It is indicated for the posterior surgical treatment of any or all of the following: degenerative disc disease (DDD) as defined by back pain of discogenic origin with degeneration of the facets with instability, trauma (i.e., fracture or dislocation), spondylolisthesis, spondylolysis, and pseudoarthrosis and failed fusions which are symptomatic or which may cause secondary instability or deformity. For transfacet fixation, the screws are inserted through the inferior articular process across the facet joint and into the pedicle. For translaminar facet fixation, the screws are inserted through the lateral aspect of the spinous process, through the lamina, through the inferior articular process, across the facet joint and into the pedicle. MRW System, Facet Screw Spinal Device U primaLOK FF
22 00813210021945 800-1501 Percutaneous Instrument Case LXH Orthopedic Manual Surgical Instrument 1 primaLOK FF
23 00813210021938 800-1500 Instrument Case LXH Orthopedic Manual Surgical Instrument 1 primaLOK FF
24 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. ODP Intervertebral Fusion Device With Bone Graft, Cervical 2 VariLift-C
25 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. ODP Intervertebral Fusion Device With Bone Graft, Cervical 2 VariLift-C
26 00813210020825 CIC2-A750 VariLift-C Unlocking Rod LXH Orthopedic Manual Surgical Instrument 1 VariLift-C
27 00813210020818 CIC2-A746 VariLift-C 10mm Trial LXH Orthopedic Manual Surgical Instrument 1 VariLift-C
28 00813210020801 CIC2-A745 VariLift-C 09mm Trial LXH Orthopedic Manual Surgical Instrument 1 VariLift-C
29 00813210020795 CIC2-A744 VariLift-C 08mm Trial LXH Orthopedic Manual Surgical Instrument 1 VariLift-C
30 00813210020788 CIC2-A743 Expander ODP Intervertebral Fusion Device With Bone Graft, Cervical 2 VariLift-C
31 00813210020771 CIC2-A742 Retainer ODP Intervertebral Fusion Device With Bone Graft, Cervical 2 VariLift-C
32 00813210020764 CIC2-A741 Inserter ODP Intervertebral Fusion Device With Bone Graft, Cervical 2 VariLift-C
33 00813210020719 CIC1-A743-C01 Expansion Wrench, T-Handle ODP Intervertebral Fusion Device With Bone Graft, Cervical 2 VariLift-C
34 00813210020702 CIC1-A741-C01 Insertion Wrench, T-Handle ODP Intervertebral Fusion Device With Bone Graft, Cervical 2 VariLift-C
35 00813210020269 CIC1-A749 Graft Ejector LXH Orthopedic Manual Surgical Instrument 1 VariLift-C
36 00813210020252 CIC1-A747 Removal Screwdriver ODP Intervertebral Fusion Device With Bone Graft, Cervical 2 VariLift-C
37 00813210020245 CIC1-A745 Tap, 9.0mm LXH Orthopedic Manual Surgical Instrument 1 VariLift-C
38 00813210020238 CIC1-A744 Tap, 7.5mm LXH Orthopedic Manual Surgical Instrument 1 VariLift-C
39 00813210020221 CIC1-A743 Expansion Wrench ODP Intervertebral Fusion Device With Bone Graft, Cervical 2 VariLift-C
40 00813210020214 CIC1-A742 Locking Wrench ODP Intervertebral Fusion Device With Bone Graft, Cervical 2 VariLift-C
41 00813210020207 CIC1-A741 Insertion Wrench ODP Intervertebral Fusion Device With Bone Graft, Cervical 2 VariLift-C
42 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. ODP Intervertebral Fusion Device With Bone Graft, Cervical 2 VariLift-C
43 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. ODP Intervertebral Fusion Device With Bone Graft, Cervical 2 VariLift-C
44 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. ODP Intervertebral Fusion Device With Bone Graft, Cervical 2 VariLift-C
45 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. ODP Intervertebral Fusion Device With Bone Graft, Cervical 2 VariLift-C
46 00813210021341 CIC2-A001 VariLift-C Instrument Case LXH Orthopedic Manual Surgical Instrument 1 VariLift-C
47 00813210022393 800-0306 Implant Sizer - 6mm LXH Orthopedic Manual Surgical Instrument 1 primaLOK-SP
48 00813210020696 CIE3-A128 Expander, 28mm MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 VariLift-LX
49 00813210020689 CIE3-A124 Expander, 24mm MAX Intervertebral Fusion Device With Bone Graft, Lumbar 2 VariLift-LX
50 00813210020672 CIE3-A026 MI Graft Impactor LXH Orthopedic Manual Surgical Instrument 1 VariLift-LX
Other products with the same Product Code "ODP"
No Primary DI Version or Model Catalog Number Device Description Brand Name Organization Name
1 M697X0341650PC1 X034-1650PC 32mm x 10mm x 16mm x 5° PLIF ASSY, Calix PC Calix Spinal Implant System XTANT MEDICAL HOLDINGS, INC.
2 M697X0341649PC1 X034-1649PC 32mm x 10mm x 15mm x 5° PLIF ASSY, Calix PC Calix Spinal Implant System XTANT MEDICAL HOLDINGS, INC.
3 M697X0341648PC1 X034-1648PC 32mm x 10mm x 14mm x 5° PLIF ASSY, Calix PC Calix Spinal Implant System XTANT MEDICAL HOLDINGS, INC.
4 M697X0341647PC1 X034-1647PC 32mm x 10mm x 13mm x 5° PLIF ASSY, Calix PC Calix Spinal Implant System XTANT MEDICAL HOLDINGS, INC.
5 M697X0341646PC1 X034-1646PC 32mm x 10mm x 12mm x 5° PLIF ASSY, Calix PC Calix Spinal Implant System XTANT MEDICAL HOLDINGS, INC.
6 M697X0341645PC1 X034-1645PC 32mm x 10mm x 11mm x 5° PLIF ASSY, Calix PC Calix Spinal Implant System XTANT MEDICAL HOLDINGS, INC.
7 M697X0341644PC1 X034-1644PC 32mm x 10mm x 10mm x 5° PLIF ASSY, Calix PC Calix Spinal Implant System XTANT MEDICAL HOLDINGS, INC.
8 M697X0341643PC1 X034-1643PC 32mm x 10mm x 9mm x 5° PLIF ASSY, Calix PC Calix Spinal Implant System XTANT MEDICAL HOLDINGS, INC.
9 M697X0341642PC1 X034-1642PC 32mm x 10mm x 8mm x 5° PLIF ASSY, Calix PC Calix Spinal Implant System XTANT MEDICAL HOLDINGS, INC.
10 M697X0341641PC1 X034-1641PC 32mm x 10mm x 7mm x 5° PLIF ASSY, Calix PC Calix Spinal Implant System XTANT MEDICAL HOLDINGS, INC.
11 M697X0341430PC1 X034-1430PC 32mm x 10mm x 16mm PLIF ASSY, Calix PC Calix Spinal Implant System XTANT MEDICAL HOLDINGS, INC.
12 M697X0341429PC1 X034-1429PC 32mm x 10mm x 15mm PLIF ASSY, Calix PC Calix Spinal Implant System XTANT MEDICAL HOLDINGS, INC.
13 M697X0341428PC1 X034-1428PC 32mm x 10mm x 14mm PLIF ASSY, Calix PC Calix Spinal Implant System XTANT MEDICAL HOLDINGS, INC.
14 M697X0341427PC1 X034-1427PC 32mm x 10mm x 13mm PLIF ASSY, Calix PC Calix Spinal Implant System XTANT MEDICAL HOLDINGS, INC.
15 M697X0341426PC1 X034-1426PC 32mm x 10mm x 12mm PLIF ASSY, Calix PC Calix Spinal Implant System XTANT MEDICAL HOLDINGS, INC.
16 M697X0341425PC1 X034-1425PC 32mm x 10mm x 11mm PLIF ASSY, Calix PC Calix Spinal Implant System XTANT MEDICAL HOLDINGS, INC.
17 M697X0341424PC1 X034-1424PC 32mm x 10mm x 10mm PLIF ASSY, Calix PC Calix Spinal Implant System XTANT MEDICAL HOLDINGS, INC.
18 M697X0341423PC1 X034-1423PC 32mm x 10mm x 9mm PLIF ASSY, Calix PC Calix Spinal Implant System XTANT MEDICAL HOLDINGS, INC.
19 M697X0341422PC1 X034-1422PC 32mm x 10mm x 8mm PLIF ASSY, Calix PC Calix Spinal Implant System XTANT MEDICAL HOLDINGS, INC.
20 M697X0341421PC1 X034-1421PC 32mm x 10mm x 7mm PLIF ASSY, Calix PC Calix Spinal Implant System XTANT MEDICAL HOLDINGS, INC.
21 M697X0341420PC1 X034-1420PC 32mm x 10mm x 6mm PLIF ASSY, Calix PC Calix Spinal Implant System XTANT MEDICAL HOLDINGS, INC.
22 M697X0340680PC1 X034-0680PC 32mm x 10mm x 16mm TLIF ASSY, Calix PC Calix Spinal Implant System XTANT MEDICAL HOLDINGS, INC.
23 M697X0340679PC1 X034-0679PC 32mm x 10mm x 15mm TLIF ASSY, Calix PC Calix Spinal Implant System XTANT MEDICAL HOLDINGS, INC.
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25 M697X0340677PC1 X034-0677PC 32mm x 10mm x 13mm TLIF ASSY, Calix PC Calix Spinal Implant System XTANT MEDICAL HOLDINGS, INC.
26 M697X0340676PC1 X034-0676PC 32mm x 10mm x 12mm TLIF ASSY, Calix PC Calix Spinal Implant System XTANT MEDICAL HOLDINGS, INC.
27 M697X0340675PC1 X034-0675PC 32mm x 10mm x 11mm TLIF ASSY, Calix PC Calix Spinal Implant System XTANT MEDICAL HOLDINGS, INC.
28 M697X0340674PC1 X034-0674PC 32mm x 10mm x 10mm TLIF ASSY, Calix PC Calix Spinal Implant System XTANT MEDICAL HOLDINGS, INC.
29 M697X0340673PC1 X034-0673PC 32mm x 10mm x 9mm TLIF ASSY, Calix PC Calix Spinal Implant System XTANT MEDICAL HOLDINGS, INC.
30 M697X0340672PC1 X034-0672PC 32mm x 10mm x 8mm TLIF ASSY, Calix PC Calix Spinal Implant System XTANT MEDICAL HOLDINGS, INC.
31 M697X0340671PC1 X034-0671PC 32mm x 10mm x 7mm TLIF ASSY, Calix PC Calix Spinal Implant System XTANT MEDICAL HOLDINGS, INC.
32 M697X0340670PC1 X034-0670PC 32mm x 10mm x 6mm TLIF ASSY, Calix PC Calix Spinal Implant System XTANT MEDICAL HOLDINGS, INC.
33 M697X0340397PC1 X034-0397PC 26mm x 10mm x 16mm, 5 degree PLIF ASSY, Calix PC Calix Spinal Implant System XTANT MEDICAL HOLDINGS, INC.
34 M697X0340396PC1 X034-0396PC 26mm x 10mm x 15mm, 5 degree PLIF ASSY, Calix PC Calix Spinal Implant System XTANT MEDICAL HOLDINGS, INC.
35 M697X0340395PC1 X034-0395PC 26mm x 10mm x 14mm, 5 degree PLIF ASSY, Calix PC Calix Spinal Implant System XTANT MEDICAL HOLDINGS, INC.
36 M697X0340394PC1 X034-0394PC 26mm x 10mm x 13mm, 5 degree PLIF ASSY, Calix PC Calix Spinal Implant System XTANT MEDICAL HOLDINGS, INC.
37 M697X0340393PC1 X034-0393PC 26mm x 10mm x 12mm, 5 degree PLIF ASSY, Calix PC Calix Spinal Implant System XTANT MEDICAL HOLDINGS, INC.
38 M697X0340392PC1 X034-0392PC 26mm x 10mm x 11mm, 5 degree PLIF ASSY, Calix PC Calix Spinal Implant System XTANT MEDICAL HOLDINGS, INC.
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41 M697X0340389PC1 X034-0389PC 26mm x 10mm x 8mm, 5 degree PLIF ASSY, Calix PC Calix Spinal Implant System XTANT MEDICAL HOLDINGS, INC.
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