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 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. ODP Intervertebral Fusion Device With Bone Graft, Cervical 2 VariLift-C
26 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
27 00813210020825 CIC2-A750 VariLift-C Unlocking Rod LXH Orthopedic Manual Surgical Instrument 1 VariLift-C
28 00813210020818 CIC2-A746 VariLift-C 10mm Trial LXH Orthopedic Manual Surgical Instrument 1 VariLift-C
29 00813210020801 CIC2-A745 VariLift-C 09mm Trial LXH Orthopedic Manual Surgical Instrument 1 VariLift-C
30 00813210020795 CIC2-A744 VariLift-C 08mm Trial LXH Orthopedic Manual Surgical Instrument 1 VariLift-C
31 00813210020788 CIC2-A743 Expander ODP Intervertebral Fusion Device With Bone Graft, Cervical 2 VariLift-C
32 00813210020771 CIC2-A742 Retainer ODP Intervertebral Fusion Device With Bone Graft, Cervical 2 VariLift-C
33 00813210020764 CIC2-A741 Inserter ODP Intervertebral Fusion Device With Bone Graft, Cervical 2 VariLift-C
34 00813210020719 CIC1-A743-C01 Expansion Wrench, T-Handle ODP Intervertebral Fusion Device With Bone Graft, Cervical 2 VariLift-C
35 00813210020702 CIC1-A741-C01 Insertion Wrench, T-Handle ODP Intervertebral Fusion Device With Bone Graft, Cervical 2 VariLift-C
36 00813210020269 CIC1-A749 Graft Ejector LXH Orthopedic Manual Surgical Instrument 1 VariLift-C
37 00813210020252 CIC1-A747 Removal Screwdriver ODP Intervertebral Fusion Device With Bone Graft, Cervical 2 VariLift-C
38 00813210020245 CIC1-A745 Tap, 9.0mm LXH Orthopedic Manual Surgical Instrument 1 VariLift-C
39 00813210020238 CIC1-A744 Tap, 7.5mm LXH Orthopedic Manual Surgical Instrument 1 VariLift-C
40 00813210020221 CIC1-A743 Expansion Wrench ODP Intervertebral Fusion Device With Bone Graft, Cervical 2 VariLift-C
41 00813210020214 CIC1-A742 Locking 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 00844856066076 64768-112 Novel Cervical Spacer, 12 mm Large, 7deg Lordotic, Titanium Novel Spinal Spacer System ALPHATEC SPINE, INC.
2 00844856066069 64768-111 Novel Cervical Spacer, 11 mm Large, 7deg Lordotic, Titanium Novel Spinal Spacer System ALPHATEC SPINE, INC.
3 00844856066052 64768-110 Novel Cervical Spacer, 10 mm Large, 7deg Lordotic, Titanium Novel Spinal Spacer System ALPHATEC SPINE, INC.
4 00844856066045 64768-109 Novel Cervical Spacer, 9 mm Large, 7deg Lordotic, Titanium Novel Spinal Spacer System ALPHATEC SPINE, INC.
5 00844856066038 64768-108 Novel Cervical Spacer, 8 mm Large, 7deg Lordotic, Titanium Novel Spinal Spacer System ALPHATEC SPINE, INC.
6 00844856066021 64768-107 Novel Cervical Spacer, 7 mm Large, 7deg Lordotic, Titanium Novel Spinal Spacer System ALPHATEC SPINE, INC.
7 00844856066014 64768-106 Novel Cervical Spacer, 6 mm Large, 7deg Lordotic, Titanium Novel Spinal Spacer System ALPHATEC SPINE, INC.
8 00844856066007 64768-105 Novel Cervical Spacer, 5 mm Large, 7deg Lordotic, Titanium Novel Spinal Spacer System ALPHATEC SPINE, INC.
9 00844856065994 64767-112 Novel Cervical Spacer, 12 mm Large, 7deg Lordotic, PEEK Novel Spinal Spacer System ALPHATEC SPINE, INC.
10 00844856065987 64767-111 Novel Cervical Spacer, 11 mm Large, 7deg Lordotic, PEEK Novel Spinal Spacer System ALPHATEC SPINE, INC.
11 00844856065970 64766-112 Novel Cervical Spacer, 12 mm Medium, 7deg Lordotic, Titanium Novel Spinal Spacer System ALPHATEC SPINE, INC.
12 00844856065963 64766-111 Novel Cervical Spacer, 11 mm Medium, 7deg Lordotic, Titanium Novel Spinal Spacer System ALPHATEC SPINE, INC.
13 00844856065956 64766-110 Novel Cervical Spacer, 10 mm Medium, 7deg Lordotic, Titanium Novel Spinal Spacer System ALPHATEC SPINE, INC.
14 00844856065949 64766-109 Novel Cervical Spacer, 9 mm Medium, 7deg Lordotic, Titanium Novel Spinal Spacer System ALPHATEC SPINE, INC.
15 00844856065932 64766-108 Novel Cervical Spacer, 8 mm Medium, 7deg Lordotic, Titanium Novel Spinal Spacer System ALPHATEC SPINE, INC.
16 00844856065925 64766-107 Novel Cervical Spacer, 7 mm Medium, 7deg Lordotic , Titanium Novel Spinal Spacer System ALPHATEC SPINE, INC.
17 00844856065918 64766-106 Novel Cervical Spacer, 6 mm Medium, 7deg Lordotic, Titanium Novel Spinal Spacer System ALPHATEC SPINE, INC.
18 00844856065901 64766-105 Novel Cervical Spacer, 5 mm Medium, 7deg Lordotic, Titanium Novel Spinal Spacer System ALPHATEC SPINE, INC.
19 00844856065895 64765-112 Novel Cervical Spacer, 12 mm Medium, 7deg Lordotic, PEEK Novel Spinal Spacer System ALPHATEC SPINE, INC.
20 00844856065888 64765-111 Novel Cervical Spacer, 11 mm Medium, 7deg Lordotic, PEEK Novel Spinal Spacer System ALPHATEC SPINE, INC.
21 00844856065871 64764-112 Novel Cervical Spacer, 12 mm Small, 7deg Lordotic ( Titanium ) Novel Spinal Spacer System ALPHATEC SPINE, INC.
22 00844856065864 64764-111 Novel Cervical Spacer, 11 mm Small, 7deg Lordotic ( Titanium ) Novel Spinal Spacer System ALPHATEC SPINE, INC.
23 00844856065857 64764-110 Novel Cervical Spacer, 10 mm Small, 7deg Lordotic ( Titanium ) Novel Spinal Spacer System ALPHATEC SPINE, INC.
24 00844856065840 64764-109 Novel Cervical Spacer, 9 mm Small, 7deg Lordotic ( Titanium ) Novel Spinal Spacer System ALPHATEC SPINE, INC.
25 00844856065833 64764-108 Novel Cervical Spacer, 8 mm Small, 7deg Lordotic ( Titanium ) Novel Spinal Spacer System ALPHATEC SPINE, INC.
26 00844856065826 64764-107 Novel Cervical Spacer, 7 mm Small, 7deg Lordotic ( Titanium ) Novel Spinal Spacer System ALPHATEC SPINE, INC.
27 00844856065819 64764-106 Novel Cervical Spacer, 6 mm Small, 7deg Lordotic ( Titanium ) Novel Spinal Spacer System ALPHATEC SPINE, INC.
28 00844856065802 64764-105 Novel Cervical Spacer, 5 mm Small, 7deg Lordotic ( Titanium ) Novel Spinal Spacer System ALPHATEC SPINE, INC.
29 00844856065796 64763-112 Novel Cervical Spacer, 12 mm Small, 7deg Lordotic Novel Spinal Spacer System ALPHATEC SPINE, INC.
30 00844856065789 64763-111 Novel Cervical Spacer, 11 mm Small, PEEK, 7deg Lordotic Novel Spinal Spacer System ALPHATEC SPINE, INC.
31 00844856053762 64907-110 Novel Cervical Trial, 10 mm Large, 7° Lordotic Novel ALPHATEC SPINE, INC.
32 00844856045392 64907-109 Novel Cervical Trial, 9 mm Large, 7° Lordotic Novel ALPHATEC SPINE, INC.
33 00844856045385 64907-108 Novel Cervical Trial, 8 mm Large, 7° Lordotic Novel ALPHATEC SPINE, INC.
34 00844856045378 64907-107 Novel Cervical Trial, 7 mm Large, 7° Lordotic Novel ALPHATEC SPINE, INC.
35 00844856045361 64907-106 Novel Cervical Trial, 6 mm Large, 7° Lordotic Novel ALPHATEC SPINE, INC.
36 00844856045354 64907-105 Novel Cervical Trial, 5 mm Large, 7° Lordotic Novel ALPHATEC SPINE, INC.
37 00844856045316 64903-110 Novel Cervical Trial, 10 mm Small/Medium, 7° Lordotic Novel ALPHATEC SPINE, INC.
38 00844856045309 64903-109 Novel Cervical Trial, 9 mm Small/Medium, 7° Lordotic Novel ALPHATEC SPINE, INC.
39 00844856045293 64903-108 Novel Cervical Trial, 8 mm Small/Medium, 7° Lordotic Novel ALPHATEC SPINE, INC.
40 00844856045286 64903-107 Novel Cervical Trial, 7 mm Small/Medium, 7° Lordotic Novel ALPHATEC SPINE, INC.
41 00844856045279 64903-106 Novel Cervical Trial, 6 mm Small/Medium, 7° Lordotic Novel ALPHATEC SPINE, INC.
42 00844856045262 64903-105 Novel Cervical Trial, 5 mm Small/Medium, 7° Lordotic Novel ALPHATEC SPINE, INC.
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44 00844856045187 64767-110 Novel Cervical Spacer, 10 mm Large, 7deg Lordotic, PEEK Novel Spinal Spacer System ALPHATEC SPINE, INC.
45 00844856045170 64767-109 Novel Cervical Spacer, 9 mm Large, 7deg Lordotic, PEEK Novel Spinal Spacer System ALPHATEC SPINE, INC.
46 00844856045163 64767-108 Novel Cervical Spacer, 8 mm Large, 7deg Lordotic, PEEK Novel Spinal Spacer System ALPHATEC SPINE, INC.
47 00844856045156 64767-107 Novel Cervical Spacer, 7 mm Large, 7deg Lordotic, PEEK Novel Spinal Spacer System ALPHATEC SPINE, INC.
48 00844856045149 64767-106 Novel Cervical Spacer, 6 mm Large, 7deg Lordotic, PEEK Novel Spinal Spacer System ALPHATEC SPINE, INC.
49 00844856045132 64767-105 Novel Cervical Spacer, 5 mm Large, 7deg Lordotic, PEEK Novel Spinal Spacer System ALPHATEC SPINE, INC.
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