| 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 | 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 |
| No | Primary DI | Version or Model | Catalog Number | Device Description | Brand Name | Organization Name |
|---|---|---|---|---|---|---|
| 1 | 00840118118378 | EZO 135 | Orthopaedic implant reamer | Removal Tool, 3.5mm | FLOWER ORTHOPEDICS CORPORATION | |
| 2 | 00840118118033 | 8804-1 | Orthopedic Manual Surgical Instrument | 1.6mm K-Wire Stabilization Sleeve | FLOWER ORTHOPEDICS CORPORATION | |
| 3 | 00840118117654 | 8548-1 | Intramedullary fixation rod and accessories | Handle, Small AO Adapter (Black) | FLOWER ORTHOPEDICS CORPORATION | |
| 4 | 00840118116466 | 8553-1 | Intramedullary fixation rod and accessories | Bone Reduction Forceps 5" curved 10mm serrated with pointed tips | FLOWER ORTHOPEDICS CORPORATION | |
| 5 | 00840118114141 | FHT 601 | FHT 601 | Flower Mini Fixed AO Handle | FlowerToe | TYBER MEDICAL LLC |
| 6 | 00840118114134 | FHT 511 | FHT 511 | Flower Mini Fixed AO Handle w/ Ø1.1mm Guidewire (6") Kit | FlowerToe | TYBER MEDICAL LLC |
| 7 | 00840118114127 | FHT 509 | FHT 509 | Flower Mini Fixed AO Handle w/ Ø0.9mm Guidewire (6") Kit | FlowerToe | TYBER MEDICAL LLC |
| 8 | 00840113230532 | 710001 | Intended to aid in the passing of sutures through bone and soft tissue during or Intended to aid in the passing of sutures through bone and soft tissue during orthopedic surgery | Green Genie Suture Passer | ASPEN SURGICAL PRODUCTS, INC. | |
| 9 | 00840113230525 | 710000NS | Intended to aid in the passing of sutures through bone and soft tissue during or Intended to aid in the passing of sutures through bone and soft tissue during orthopedic surgery | Hoffee Suture Retriever | ASPEN SURGICAL PRODUCTS, INC. | |
| 10 | 00840113230518 | 710000 | Intended to aid in the passing of sutures through bone and soft tissue during or Intended to aid in the passing of sutures through bone and soft tissue during orthopedic surgery | Hoffee Suture Retriever | ASPEN SURGICAL PRODUCTS, INC. | |
| 11 | 00840113221066 | 101000PBX | Single use device intended to cover exposed ends of orthopedic pin and k-wires t Single use device intended to cover exposed ends of orthopedic pin and k-wires to help protect the exposed wire from snagging on clothing. | Oxboro™ Pin Cover | ASPEN SURGICAL PRODUCTS, INC. | |
| 12 | 00840113221042 | 101001BBG | Single use device intended to cover exposed ends of orthopedic pin and k-wires t Single use device intended to cover exposed ends of orthopedic pin and k-wires to help protect the exposed wire from snagging on clothing. | Oxboro™ Pin Cover | ASPEN SURGICAL PRODUCTS, INC. | |
| 13 | 00840113221028 | 101001PBX | Single use device intended to cover exposed ends of orthopedic pin and k-wires t Single use device intended to cover exposed ends of orthopedic pin and k-wires to help protect the exposed wire from snagging on clothing. | Oxboro™ Pin Cover | ASPEN SURGICAL PRODUCTS, INC. | |
| 14 | 00840113221004 | 101002PBX | Single use device intended to cover exposed ends of orthopedic pin and k-wires t Single use device intended to cover exposed ends of orthopedic pin and k-wires to help protect the exposed wire from snagging on clothing. | Oxboro™ Pin Cover | ASPEN SURGICAL PRODUCTS, INC. | |
| 15 | 00840113220991 | 101003PBX | Single use device intended to cover exposed ends of orthopedic pin and k-wires t Single use device intended to cover exposed ends of orthopedic pin and k-wires to help protect the exposed wire from snagging on clothing. | Oxboro™ Pin Cover | ASPEN SURGICAL PRODUCTS, INC. | |
| 16 | 00840097504926 | 4100-002-0102 | Anatomic Cotton Kit, 10/12mm Thickness | restor3d Disposable Instrument Kit | RESTOR3D | |
| 17 | 00840097504919 | 4100-002-0101 | Anatomic Cotton Kit, 5-8mm Thickness | restor3d Disposable Instrument Kit | RESTOR3D | |
| 18 | 00840097504902 | 4110-S023 | Cervical Trial Kit without Stop, Large Footprint, 5-10mm Thickness, 7 Degree | restor3d Disposable Instrument Kit | RESTOR3D | |
| 19 | 00840097504896 | 4110-S022 | Cervical Trial Kit without Stop, Medium Footprint, 5-10mm Thickness, 7 Degree | restor3d Disposable Instrument Kit | RESTOR3D | |
| 20 | 00840097504889 | 4110-S021 | Cervical Trial Kit without Stop, Small Footprint, 5-10mm Thickness, 7 Degree | restor3d Disposable Instrument Kit | RESTOR3D | |
| 21 | 00840097504872 | 4110-S013 | Cervical Trial Kit with Stop, Large Footprint, 5-10mm Height, 7 degree | restor3d Disposable Instrument Kit | RESTOR3D | |
| 22 | 00840097504865 | 4110-S012 | Cervical Trial Kit with Stop, Medium Footprint, 5-10mm Height, 7 degree | restor3d Disposable Instrument Kit | RESTOR3D | |
| 23 | 00840097504858 | 4110-S011 | Cervical Trial Kit with Stop, Small Footprint, 5-10mm Height, 7 degree | restor3d Disposable Instrument Kit | RESTOR3D | |
| 24 | 00840097504636 | 6105-2723141005 | Titanium (Ti-6Al-4V) Subtalar Wedge, Left Foot, Large Footprint, 14mm Thickness, 5 Degree | restor3d Disposable Instrument, Wedge Trial | RESTOR3D | |
| 25 | 00840097504629 | 6105-2723140005 | Disposable Trial, Subtalar Wedge, Large Footprint, 14 mm thickness, 0 degree | restor3d Disposable Instrument, Wedge Trial | RESTOR3D | |
| 26 | 00840097504612 | 6105-2723101005 | Disposable Trial, Subtalar Wedge, Large Footprint, 10 mm thickness, 10 degree | restor3d Disposable Instrument, Wedge Trial | RESTOR3D | |
| 27 | 00840097504605 | 6105-2723100005 | Disposable Trial, Subtalar Wedge, Large Footprint, 10 mm thickness, 0 degree | restor3d Disposable Instrument, Wedge Trial | RESTOR3D | |
| 28 | 00840097504599 | 6105-2719141005 | Disposable Trial, Subtalar Wedge, Small Footprint, 14 mm thickness, 10 degree | restor3d Disposable Instrument, Wedge Trial | RESTOR3D | |
| 29 | 00840097504582 | 6105-2719140005 | Disposable Trial, Subtalar Wedge, Small Footprint, 14 mm thickness, 0 degree | restor3d Disposable Instrument, Wedge Trial | RESTOR3D | |
| 30 | 00840097504575 | 6105-2719101005 | Disposable Trial, Subtalar Wedge, Small Footprint, 10 mm thickness, 10 degree | restor3d Disposable Instrument, Wedge Trial | RESTOR3D | |
| 31 | 00840097504568 | 6105-2719100005 | Disposable Trial, Subtalar Wedge, Small Footprint, 10 mm thickness, 0 degree | restor3d Disposable Instrument, Wedge Trial | RESTOR3D | |
| 32 | 00840097504551 | 6110-N01-KTL01NST | Disposable Trial, Cervical Trial Kit w/o Stop, Large Footprint | restor3d Disposable Instrument, Cervical Cage Trial | RESTOR3D | |
| 33 | 00840097504544 | 6110-N01-KTM01NST | Disposable Trial, Cervical Trial Kit w/o Stop, Medium Footprint | restor3d Disposable Instrument, Cervical Cage Trial | RESTOR3D | |
| 34 | 00840097504537 | 6110-N01-KTS01NST | Disposable Trial, Cervical Trial Kit w/o Stop, Small Footprint | restor3d Disposable Instrument, Cervical Cage Trial | RESTOR3D | |
| 35 | 00840097504520 | 6110-N01-KTL01 | Disposable Trial, Cervical Trial Kit w/ Stop, Large Footprint | restor3d Disposable Instrument, Cervical Cage Trial | RESTOR3D | |
| 36 | 00840097504513 | 6110-N01-KTM01 | Disposable Trial, Cervical Trial Kit w/ Stop, Medium Footprint | restor3d Disposable Instrument, Cervical Cage Trial | RESTOR3D | |
| 37 | 00840097504506 | 6110-N01-KTS01 | Disposable Trial, Cervical Trial Kit w/ Stop, Small Footprint | restor3d Disposable Instrument, Cervical Cage Trial | RESTOR3D | |
| 38 | 00840097503233 | 6101-NSP-C1012 | Non-Sterile Disposable Instrument, Evans Wedge, Double Sided, Large Footprint, 1 Non-Sterile Disposable Instrument, Evans Wedge, Double Sided, Large Footprint, 10/12mm Thickness | restor3d Disposable Instrument, Wedge Trial | RESTOR3D | |
| 39 | 00840097503226 | 6101-NSP-C0810 | Non-Sterile Disposable Instrument, Evans Wedge, Double Sided, Large Footprint, 0 Non-Sterile Disposable Instrument, Evans Wedge, Double Sided, Large Footprint, 08/10mm Thickness | restor3d Disposable Instrument, Wedge Trial | RESTOR3D | |
| 40 | 00840097503219 | 6101-NSP-B1012 | Non-Sterile Disposable Instrument, Evans Wedge, Double Sided, Medium Footprint, Non-Sterile Disposable Instrument, Evans Wedge, Double Sided, Medium Footprint, 10/12mm Thickness | restor3d Disposable Instrument, Wedge Trial | RESTOR3D | |
| 41 | 00840097503202 | 6101-NSP-B0810 | Non-Sterile Disposable Instrument, Evans Wedge, Double Sided, Medium Footprint, Non-Sterile Disposable Instrument, Evans Wedge, Double Sided, Medium Footprint, 8/10mm Thickness | restor3d Disposable Instrument, Wedge Trial | RESTOR3D | |
| 42 | 00840097503196 | 6101-NSP-A1012 | Non-Sterile Disposable Instrument, Evans Wedge, Double Sided, Small Footprint, 1 Non-Sterile Disposable Instrument, Evans Wedge, Double Sided, Small Footprint, 10/12mm Thickness | restor3d Disposable Instrument, Wedge Trial | RESTOR3D | |
| 43 | 00840097503189 | 6101-NSP-A0810 | Non-Sterile Disposable Instrument, Evans Wedge, Double Sided, Small Footprint, 8 Non-Sterile Disposable Instrument, Evans Wedge, Double Sided, Small Footprint, 8/10mm Thickness | restor3d Disposable Instrument, Wedge Trial | RESTOR3D | |
| 44 | 00840097503172 | 6100-N02-A0910 | Non-Sterile Disposable Instrument, Cotton Wedge 002, Double Sided, 9/10mm Thickness | restor3d Disposable Instrument, Wedge Trial | RESTOR3D | |
| 45 | 00840097503165 | 6100-N02-A0708 | Non-Sterile Disposable Instrument, Cotton Wedge 002, Double Sided, 7/8mm Thickness | restor3d Disposable Instrument, Wedge Trial | RESTOR3D | |
| 46 | 00840097503158 | 6100-N02-A0506 | Non-Sterile Disposable Instrument, Cotton Wedge 002, Double Sided, 5/6mm Thickness | restor3d Disposable Instrument, Wedge Trial | RESTOR3D | |
| 47 | 00840097503141 | 6100-NSP-B0506 | Non-Sterile Disposable Instrument, Cotton Wedge, Double Sided, Medium Footprint Non-Sterile Disposable Instrument, Cotton Wedge, Double Sided, Medium Footprint 5/6mm Thickness | restor3d Disposable Instrument, Wedge Trial | RESTOR3D | |
| 48 | 00840097503134 | 6100-NSP-B0405 | Non-Sterile Disposable Instrument, Cotton Wedge, Double Sided, Medium Footprint, Non-Sterile Disposable Instrument, Cotton Wedge, Double Sided, Medium Footprint, 4/5mm Thickness | restor3d Disposable Instrument, Wedge Trial | RESTOR3D | |
| 49 | 00840097503127 | 6100-NSP-A0506 | Non-Sterile Disposable Instrument, Cotton Wedge, Double Sided, Small Footprint, Non-Sterile Disposable Instrument, Cotton Wedge, Double Sided, Small Footprint, 5/6mm Thickness | restor3d Disposable Instrument, Wedge Trial | RESTOR3D | |
| 50 | 00840097503110 | 6100-NSP-A0405 | Non-Sterile Disposable Instrument, Cotton Wedge, Double Sided, Small Footprint, Non-Sterile Disposable Instrument, Cotton Wedge, Double Sided, Small Footprint, 4/5mm Thickness | restor3d Disposable Instrument, Wedge Trial | RESTOR3D |