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 00813210020207 CIC1-A741 Insertion Wrench ODP Intervertebral Fusion Device With Bone Graft, Cervical 2 VariLift-C
43 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
44 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
45 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
46 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
47 00813210021341 CIC2-A001 VariLift-C Instrument Case LXH Orthopedic Manual Surgical Instrument 1 VariLift-C
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 "LXH"
No Primary DI Version or Model Catalog Number Device Description Brand Name Organization Name
1 09421028116817 ENZUGRIP ENZUGRIP A reusable manual surgical instrument intended to be used during an orthopaedic A reusable manual surgical instrument intended to be used during an orthopaedic surgical procedure Microport Broach Handle - Removable Grip ENZTEC LIMITED
2 09421028116800 ATCENZN1 ATCENZN1 A reusable manual surgical instrument intended to be used during an orthopaedic A reusable manual surgical instrument intended to be used during an orthopaedic surgical procedure Microport Single Offset Broach Handle ENZTEC LIMITED
3 09421028116442 LET30220T LET30220T Intended to be used for the insertion of spinal implants into the spinal space d Intended to be used for the insertion of spinal implants into the spinal space during total artificial disc replacement surgery. CONDUIT LLIF Slide Inserter 12-14mm ENZTEC LIMITED
4 09421028116435 LET30210T LET30210T Intended to be used for the insertion of spinal implants into the spinal space d Intended to be used for the insertion of spinal implants into the spinal space during total artificial disc replacement surgery. CONDUIT LLIF Slide Inserter 8-10mm ENZTEC LIMITED
5 09421028116374 9095.11.013 9095.11.013 A reusable manual surgical instrument intended to be used during an orthopaedic A reusable manual surgical instrument intended to be used during an orthopaedic surgical procedure Dual Offset Broach Handle F1 Connection - Right ENZTEC LIMITED
6 09421028116367 9095.11.014 9095.11.014 A reusable manual surgical instrument intended to be used during an orthopaedic A reusable manual surgical instrument intended to be used during an orthopaedic surgical procedure Dual Offset Broach Handle F1 Connection - Left ENZTEC LIMITED
7 09421028116343 000-0563 000-0563 A reusable manual surgical instrument intended to be used during an orthopaedic A reusable manual surgical instrument intended to be used during an orthopaedic surgical procedure Fine Adjustment Cutting Guide - Mini Screw Driver ENZTEC LIMITED
8 09421028114202 ATCENZR2 ATCENZR2 A reusable manual surgical instrument intended to be used during an orthopaedic A reusable manual surgical instrument intended to be used during an orthopaedic surgical procedure Microport Double Offset Broach Handle - Right ENZTEC LIMITED
9 09421028114196 ATCENZL2 ATCENZL2 A reusable manual surgical instrument intended to be used during an orthopaedic A reusable manual surgical instrument intended to be used during an orthopaedic surgical procedure Microport Double Offset Broach Handle - Left ENZTEC LIMITED
10 09421028113465 72205272 72205272 Intended to be used for the preparation and pre-tensioning of single tendon graf Intended to be used for the preparation and pre-tensioning of single tendon grafts for ligament reconstruction X-Wing Sliding Base ENZTEC LIMITED
11 09421028113458 72205271 72205271 Intended to be used for the preparation and pre-tensioning of single tendon graf Intended to be used for the preparation and pre-tensioning of single tendon grafts for ligament reconstruction X-Wing Tensioner ENZTEC LIMITED
12 09421028113441 72205270 72205270 Intended to be used for the preparation and pre-tensioning of single tendon graf Intended to be used for the preparation and pre-tensioning of single tendon grafts for ligament reconstruction. X-Wing Base ENZTEC LIMITED
13 09421028111959 72205274 72205274 Intended to be used for the preparation and pre-tensioning of single tendon graf Intended to be used for the preparation and pre-tensioning of single tendon grafts for ligament reconstruction Button Holder - Suture Management ENZTEC LIMITED
14 09421028111942 72205273 72205273 Intended to be used for the preparation and pre-tensioning of single tendon graf Intended to be used for the preparation and pre-tensioning of single tendon grafts for ligament reconstruction Button Holder ENZTEC LIMITED
15 09421028111669 9095.11.002 9095.11.002 A reusable manual surgical instrument intended to be used during an orthopaedic A reusable manual surgical instrument intended to be used during an orthopaedic surgical procedure HMAX Dual Offset Broach Handle Right ENZTEC LIMITED
16 09421028111652 9095.11.003 9095.11.003 A reusable manual surgical instrument intended to be used during an orthopaedic A reusable manual surgical instrument intended to be used during an orthopaedic surgical procedure HMAX Dual Offset Broach Handle Left ENZTEC LIMITED
17 09421028111218 4240-4303 4240-4303 A reusable manual surgical instrument intended to be used during an orthopaedic A reusable manual surgical instrument intended to be used during an orthopaedic surgical procedure Enztec Patella Shim - 3mm ENZTEC LIMITED
18 09421028111201 4240-4302 4240-4302 A reusable manual surgical instrument intended to be used during an orthopaedic A reusable manual surgical instrument intended to be used during an orthopaedic surgical procedure Enztec Patella Shim - 2mm ENZTEC LIMITED
19 09421028111195 4240-4301 4240-4301 A reusable manual surgical instrument intended to be used during an orthopaedic A reusable manual surgical instrument intended to be used during an orthopaedic surgical procedure Enztec Patella Shim - 1mm ENZTEC LIMITED
20 09353903009016 APN000265 NXLH/1 FO Large Quick Coupling Ratcheting Surgical Handle 1/pkg FO NX Nail System FIELD ORTHOPAEDICS PTY LTD
21 09353903002666 CPN000052 BTSC00043 2.0 FO Guide Sleeve FO Micro Screw System FIELD ORTHOPAEDICS PTY LTD
22 09353903002659 CPN000051 BTSC00042 1.6 FO Guide Sleeve FO Micro Screw System FIELD ORTHOPAEDICS PTY LTD
23 09353903002642 CPN000050 BTSC00041 1.2 FO Guide Sleeve FO Micro Screw System FIELD ORTHOPAEDICS PTY LTD
24 09353903002635 CPN000049 BTSC00040 1.0 FO Guide Sleeve FO Micro Screw System FIELD ORTHOPAEDICS PTY LTD
25 09353903002628 CPN000048 BTSC00039 0.8 FO Guide Sleeve FO Micro Screw System FIELD ORTHOPAEDICS PTY LTD
26 09353903002611 CPN000047 BTSC00038 0.6 FO Guide Sleeve FO Micro Screw System FIELD ORTHOPAEDICS PTY LTD
27 09353903002543 SPN000005 BTSC00031 FO Soft Tissue Protector FO Micro Screw System FIELD ORTHOPAEDICS PTY LTD
28 09353903002536 SPN000004 BTSC00030 FO Surgical Handle, Quick Coupling FO Micro Screw System FIELD ORTHOPAEDICS PTY LTD
29 09353903002529 CPN000029 BTSC00029 FO Micro Hex Driver (Cannulated) FO Micro Screw System FIELD ORTHOPAEDICS PTY LTD
30 09353903001799 CPN000059 BTSC00076 0.6mm Wire Collet Insert FO Micro Screw System FIELD ORTHOPAEDICS PTY LTD
31 09353903001782 CPN000058 BTSC00075 0.6mm Pin Collet Insert FO Micro Screw System FIELD ORTHOPAEDICS PTY LTD
32 09353903000426 FOGS-0020 FOGS-0020/1 2.0 FO Guide Sleeve FO Micro Screw System FIELD ORTHOPAEDICS PTY LTD
33 09353903000419 FOGS-0016 FOGS-0016/1 1.6 FO Guide Sleeve FO Micro Screw System FIELD ORTHOPAEDICS PTY LTD
34 09353903000402 FOGS-0012 FOGS-0012/1 1.2 FO Guide Sleeve FO Micro Screw System FIELD ORTHOPAEDICS PTY LTD
35 09353903000396 FOGS-0010 FOGS-0010/1 1.0 FO Guide Sleeve FO Micro Screw System FIELD ORTHOPAEDICS PTY LTD
36 09353903000389 FOGS-0008 FOGS-0008/1 0.8 FO Guide Sleeve FO Micro Screw System FIELD ORTHOPAEDICS PTY LTD
37 09353903000372 FOGS-0006 FOGS-0006/1 0.6 FO Guide Sleeve FO Micro Screw System FIELD ORTHOPAEDICS PTY LTD
38 09353903000303 MSTP-0000 MSTP-0000/1 FO Soft Tissue Protector FO Micro Screw System FIELD ORTHOPAEDICS PTY LTD
39 09353903000297 MSHD-0000 MSHD-0000/1 FO Surgical Handle, Quick Coupling FO Micro Screw System FIELD ORTHOPAEDICS PTY LTD
40 09353903000280 MSHX-0000 MSHX-0000/1 FO Micro Hex Driver (Cannulated) FO Micro Screw System FIELD ORTHOPAEDICS PTY LTD
41 09348215113308 199-112-172 Cup Impactor SIGNATURE ORTHOPAEDICS PTY LTD
42 09348215109448 112-172-915 World Cup Curved Inserter - Tip SIGNATURE ORTHOPAEDICS PTY LTD
43 09348215105228 111-45-2012 Everglade Broach SIGNATURE ORTHOPAEDICS PTY LTD
44 09348215105211 111-45-2011 Everglade Broach SIGNATURE ORTHOPAEDICS PTY LTD
45 09348215105204 111-45-2010 Everglade Broach SIGNATURE ORTHOPAEDICS PTY LTD
46 09348215105198 111-45-2009 Everglade Broach SIGNATURE ORTHOPAEDICS PTY LTD
47 09348215105181 111-45-2008 Everglade Broach SIGNATURE ORTHOPAEDICS PTY LTD
48 09348215105174 111-45-2007 Everglade Broach SIGNATURE ORTHOPAEDICS PTY LTD
49 09348215105167 111-45-2006 Everglade Broach SIGNATURE ORTHOPAEDICS PTY LTD
50 09348215105150 111-45-2005 Everglade Broach SIGNATURE ORTHOPAEDICS PTY LTD