No | Primary DI | Version or Model | Catalog Number | Device Description | Product Code | Product Code Name | Device Class | Brand Name |
---|---|---|---|---|---|---|---|---|
1 | 00880304547643 | 32-422777 | 32-422777 | LXH | ORTHOPEDIC MANUAL SURGICAL INSTRUMENT | 1 | Oxford® Uni Knee System | |
2 | 00880304525658 | 32-422760 | 32-422760 | LXH | ORTHOPEDIC MANUAL SURGICAL INSTRUMENT | 1 | Oxford Uni Knee System | |
3 | 00880304525641 | 32-422812 | 32-422812 | LXH | ORTHOPEDIC MANUAL SURGICAL INSTRUMENT | 1 | Oxford Uni Knee System | |
4 | 00880304525634 | 32-422811 | 32-422811 | LXH | ORTHOPEDIC MANUAL SURGICAL INSTRUMENT | 1 | Oxford Uni Knee System | |
5 | 00880304525542 | 32-422802 | 32-422802 | LXH | ORTHOPEDIC MANUAL SURGICAL INSTRUMENT | 1 | Oxford Uni Knee System | |
6 | 00880304525535 | 32-422806 | 32-422806 | LXH | ORTHOPEDIC MANUAL SURGICAL INSTRUMENT | 1 | Oxford Uni Knee System | |
7 | 00880304525467 | 32-422803 | 32-422803 | LXH | ORTHOPEDIC MANUAL SURGICAL INSTRUMENT | 1 | Oxford Uni Knee System | |
8 | 00880304525450 | 32-423231 | 32-423231 | LXH | ORTHOPEDIC MANUAL SURGICAL INSTRUMENT | 1 | Oxford Uni Knee System | |
9 | 00880304525443 | 32-422771 | 32-422771 | LXH | ORTHOPEDIC MANUAL SURGICAL INSTRUMENT | 1 | Oxford Uni Knee System | |
10 | 00880304525436 | 32-422805 | 32-422805 | LXH | ORTHOPEDIC MANUAL SURGICAL INSTRUMENT | 1 | Oxford Uni Knee System | |
11 | 00880304525429 | 32-423223 | 32-423223 | LXH | ORTHOPEDIC MANUAL SURGICAL INSTRUMENT | 1 | Oxford Uni Knee System | |
12 | 00880304525412 | 32-422804 | 32-422804 | LXH | ORTHOPEDIC MANUAL SURGICAL INSTRUMENT | 1 | Oxford Uni Knee System | |
13 | 00880304525382 | 32-422801 | 32-422801 | LXH | ORTHOPEDIC MANUAL SURGICAL INSTRUMENT | 1 | Oxford Uni Knee System | |
14 | 00880304509696 | 32-422977 | 32-422977 | LXH | ORTHOPEDIC MANUAL SURGICAL INSTRUMENT | 1 | Oxford Uni Knee System | |
15 | 00880304504714 | 32-422845 | 32-422845 | HTW | BIT, DRILL | 1 | Oxford Uni Knee System | |
16 | 00880304504707 | 32-423228 | 32-423228 | HTW | BIT, DRILL | 1 | Oxford® Uni Knee System | |
17 | 00880304007581 | 595250 | 595250 | FSM | TRAY, SURGICAL, INSTRUMENT | 1 | MICROPLASTY HIP | |
18 | 05019279999439 | 154373 | 154373 | HRY | PROSTHESIS, KNEE, FEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, METAL/POLYMER | 2 | OXFORD PARTIAL KNEE SYSTEM | |
19 | 05019279999422 | 154372 | 154372 | HRY | PROSTHESIS, KNEE, FEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, METAL/POLYMER | 2 | OXFORD PARTIAL KNEE SYSTEM | |
20 | 05019279999415 | 154371 | 154371 | HRY | PROSTHESIS, KNEE, FEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, METAL/POLYMER | 2 | OXFORD PARTIAL KNEE SYSTEM | |
21 | 05019279999453 | 154375 | 154375 | HRY | PROSTHESIS, KNEE, FEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, METAL/POLYMER | 2 | OXFORD PARTIAL KNEE SYSTEM | |
22 | 05019279999446 | 154374 | 154374 | HRY | PROSTHESIS, KNEE, FEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, METAL/POLYMER | 2 | OXFORD PARTIAL KNEE SYSTEM | |
23 | 05019279999491 | 154379 | 154379 | HRY | PROSTHESIS, KNEE, FEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, METAL/POLYMER | 2 | OXFORD PARTIAL KNEE SYSTEM | |
24 | 05019279999484 | 154378 | 154378 | HRY | PROSTHESIS, KNEE, FEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, METAL/POLYMER | 2 | OXFORD PARTIAL KNEE SYSTEM | |
25 | 05019279999477 | 154377 | 154377 | HRY | PROSTHESIS, KNEE, FEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, METAL/POLYMER | 2 | OXFORD PARTIAL KNEE SYSTEM | |
26 | 05019279999460 | 154376 | 154376 | HRY | PROSTHESIS, KNEE, FEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, METAL/POLYMER | 2 | OXFORD PARTIAL KNEE SYSTEM | |
27 | 05019279998319 | 110028563 | 110028563 | GAD | RETRACTOR | 1 | ASI INSTRUMENTSCOBRA STYLE RETRACTOR | |
28 | 05019279924271 | 31-500960 | 31-500960 | HWT | TEMPLATE | 1 | RECAP HIP INSTRUMENTATION | |
29 | 05019279924257 | 31-500958 | 31-500958 | HWT | TEMPLATE | 1 | RECAP HIP INSTRUMENTATION | |
30 | 05019279924233 | 31-500956 | 31-500956 | HWT | TEMPLATE | 1 | RECAP HIP INSTRUMENTATION | |
31 | 05019279924219 | 31-500954 | 31-500954 | HWT | TEMPLATE | 1 | RECAP HIP INSTRUMENTATION | |
32 | 05019279924196 | 31-500952 | 31-500952 | HWT | TEMPLATE | 1 | RECAP HIP INSTRUMENTATION | |
33 | 05019279924172 | 31-500950 | 31-500950 | HWT | TEMPLATE | 1 | RECAP HIP INSTRUMENTATION | |
34 | 05019279924158 | 31-500948 | 31-500948 | HWT | TEMPLATE | 1 | RECAP HIP INSTRUMENTATION | |
35 | 05019279924134 | 31-500946 | 31-500946 | HWT | TEMPLATE | 1 | RECAP HIP INSTRUMENTATION | |
36 | 05019279924110 | 31-500944 | 31-500944 | HWT | TEMPLATE | 1 | RECAP HIP INSTRUMENTATION | |
37 | 05019279924097 | 31-500942 | 31-500942 | HWT | TEMPLATE | 1 | RECAP HIP INSTRUMENTATION | |
38 | 05019279924073 | 31-500940 | 31-500940 | HWT | TEMPLATE | 1 | RECAP HIP INSTRUMENTATION | |
39 | 05019279924059 | 31-500938 | 31-500938 | HWT | TEMPLATE | 1 | RECAP HIP INSTRUMENTATION | |
40 | 05019279924011 | 31-500760 | 31-500760 | HTO | REAMER | 1 | RECAP HIP INSTRUMENTATION | |
41 | 05019279924004 | 31-500758 | 31-500758 | HTO | REAMER | 1 | RECAP HIP INSTRUMENTATION | |
42 | 05019279923991 | 31-500756 | 31-500756 | HTO | REAMER | 1 | RECAP HIP INSTRUMENTATION | |
43 | 05019279923984 | 31-500754 | 31-500754 | HTO | REAMER | 1 | RECAP HIP INSTRUMENTATION | |
44 | 05019279923977 | 31-500752 | 31-500752 | HTO | REAMER | 1 | RECAP HIP INSTRUMENTATION | |
45 | 05019279923960 | 31-500750 | 31-500750 | HTO | REAMER | 1 | RECAP HIP INSTRUMENTATION | |
46 | 05019279923953 | 31-500748 | 31-500748 | HTO | REAMER | 1 | RECAP HIP INSTRUMENTATION | |
47 | 05019279923946 | 31-500746 | 31-500746 | HTO | REAMER | 1 | RECAP HIP INSTRUMENTATION | |
48 | 05019279923939 | 31-500744 | 31-500744 | HTO | REAMER | 1 | RECAP HIP INSTRUMENTATION | |
49 | 05019279923922 | 31-500742 | 31-500742 | HTO | REAMER | 1 | RECAP HIP INSTRUMENTATION | |
50 | 05019279923915 | 31-500740 | 31-500740 | HTO | REAMER | 1 | RECAP HIP INSTRUMENTATION |
No | Primary DI | Version or Model | Catalog Number | Device Description | Brand Name | Organization Name |
---|---|---|---|---|---|---|
1 | 00811801039690 | CI-10076-02 | CIS TRIAL/TRESTLE DRILL GUIDE, 6-12MM | Novel | ALPHATEC SPINE, INC. | |
2 | 00811801039140 | CI-10348 | Set Screw Alignment Tube | General Instruments | ALPHATEC SPINE, INC. | |
3 | 00811801037733 | CI-10431 | Variable Angle Drill Guide, Cervical | General Instruments | ALPHATEC SPINE, INC. | |
4 | 00811801035081 | CI-10162-02 | Dual-lead Illico Screw Extender - Distal Bridge | Illico | ALPHATEC SPINE, INC. | |
5 | 00811801035074 | CI-10162-01 | Dual-lead Illico Screw Extender | Illico | ALPHATEC SPINE, INC. | |
6 | 00811801034954 | CI-10171 | Double Barrel Variable Drill Guide, Standard Drill | General Instruments | ALPHATEC SPINE, INC. | |
7 | 00811801032660 | CI-10144 | Adjustable Drill guide | General Instruments | ALPHATEC SPINE, INC. | |
8 | 00811801032493 | CI-10057 | Adjustable Drill guide | General Instruments | ALPHATEC SPINE, INC. | |
9 | 00811801032356 | CI-10105 | CBx Drill Guide | Arsenal | ALPHATEC SPINE, INC. | |
10 | 00811801032318 | CI-10076-08 | CIS TRIAL/TRESTLE DRILL GUIDE, 12-18MM | Novel | ALPHATEC SPINE, INC. | |
11 | 00811801032301 | CI-10076-07 | CIS TRIAL/TRESTLE DRILL GUIDE, 11-16MM | Novel | ALPHATEC SPINE, INC. | |
12 | 00811801032295 | CI-10076-06 | CIS TRIAL/TRESTLE DRILL GUIDE, 10-16MM | Novel | ALPHATEC SPINE, INC. | |
13 | 00811801032288 | CI-10076-05 | CIS TRIAL/TRESTLE DRILL GUIDE, 9-14MM | Novel | ALPHATEC SPINE, INC. | |
14 | 00811801032271 | CI-10076-04 | CIS TRIAL/TRESTLE DRILL GUIDE, 8-14MM | Novel | ALPHATEC SPINE, INC. | |
15 | 00811801032264 | CI-10076-03 | CIS TRIAL/TRESTLE DRILL GUIDE, 7-12MM | Novel | ALPHATEC SPINE, INC. | |
16 | 00811801032240 | CI-10076-01 | CIS TRIAL/TRESTLE DRILL GUIDE, 5-12MM | Novel | ALPHATEC SPINE, INC. | |
17 | 00811801031861 | CI-10055 | Set Screw Loader Tube for Arsenal | Arsenal | ALPHATEC SPINE, INC. | |
18 | 00811801031854 | CI-10054 | Tighter ID Solanas Drill Guide | Solanas | ALPHATEC SPINE, INC. | |
19 | 00811801031694 | CI-10029 | Trestle Luxe Variable Drill Guide | Trestle Luxe | ALPHATEC SPINE, INC. | |
20 | 00811801031687 | CI-10028 | Trestle Luxe Fixed Drill Guide | Trestle Luxe | ALPHATEC SPINE, INC. | |
21 | 00811801031205 | CI-10100 | Set Screw Loader Tube for Arsenal | Arsenal | ALPHATEC SPINE, INC. | |
22 | 00811801030239 | CI-10024 | Illico Screw Extenders | Illico | ALPHATEC SPINE, INC. | |
23 | 00810482031429 | 9300-LI01 | The Blustone Synergy Magma System is implanted using a combination of device spe The Blustone Synergy Magma System is implanted using a combination of device specific and universal class I instruments manufactured from stainless steel materials that conform to ASTM F899. The Magma lateral implant inserter is designed to allow for disassembly during cleaning and sterilization.Instructions regarding disassembly, cleaning and sterilization of the inserter instrument are provided in the product insert. | Blustone Synergy Lumbar Lateral Inserter (Magma) | BLUSTONE SYNERGY, LLC | |
24 | 00810482031405 | 9200-PI01 | The BluStone Synergy Basalt System is implanted using a combination of device sp The BluStone Synergy Basalt System is implanted using a combination of device specific and universal class I instruments manufactured from stainless steel materials that conform to ASTM F899. The Basalt PLIF implant inserter is designed to allow for disassembly during cleaning and sterilization.Instructions regarding disassembly, cleaning and sterilization of the inserter/pusher instrument are provided in the product insert. | Blustone Synergy Lumbar PLIF Inserter (Basalt) | BLUSTONE SYNERGY, LLC | |
25 | 00810482031382 | 9100-TI01 | The BluStone Synergy Obsidian System is implanted using a combination of device The BluStone Synergy Obsidian System is implanted using a combination of device specific and universal class I instruments manufactured from stainless steel materials that conform to ASTM F899. The Obsidian TLIF implant inserter/pusher is designed to allow for disassembly during cleaning and sterilization.Instructions regarding disassembly, cleaning and sterilization of the inserter/pusher instrument are provided in the product insert. | Blustone Synergy Lumbar TLIF Inserter/Pusher (Obsidian) | BLUSTONE SYNERGY, LLC | |
26 | 00810482030651 | 9000-CI01 | The Blustone Synergy Cervical Interbody Fusion System is implanted using a combi The Blustone Synergy Cervical Interbody Fusion System is implanted using a combination of device specific and universal class I instruments manufactured from stainless steel materials that conform to ASTM F899. The cervical implant inserter is designed to allow for disassembly during cleaning and sterilization.Instructions regarding disassembly of the inserter instrument are provided in the product insert. | Blustone Synergy Cervical Inserter | BLUSTONE SYNERGY, LLC | |
27 | 00810111221023 | 1405-2164 | Drill Sleeve | Drill Sleeve | TREACE MEDICAL CONCEPTS, INC. | |
28 | 00810111220545 | 1405-2610 | Rotational Guide | Rotational Guide | TREACE MEDICAL CONCEPTS, INC. | |
29 | 00810111220309 | 1405-2539 | Staple Drill Guide | Drill Guide | TREACE MEDICAL CONCEPTS, INC. | |
30 | 00810111220019 | 1405-2456 | Staple Drill Guide | Drill Guide | TREACE MEDICAL CONCEPTS, INC. | |
31 | 00810111220002 | 1405-2455 | Staple Drill Guide | Drill Guide | TREACE MEDICAL CONCEPTS, INC. | |
32 | 00810055070923 | F10342-1017T | The Shaped Cutting Template is a reusable stainless steel surgical instrument. T The Shaped Cutting Template is a reusable stainless steel surgical instrument. The Shaped Cutting Template is intended to allow users to trace and cut specific shapes of implantable materials, such as the OviTex Reinforced Tissue Matrix. | OviTex® | TELA BIO, INC. | |
33 | 00810055070916 | F10341-1016T | The Shaped Cutting Template is a reusable stainless steel surgical instrument. T The Shaped Cutting Template is a reusable stainless steel surgical instrument. The Shaped Cutting Template is intended to allow users to trace and cut specific shapes of implantable materials, such as the OviTex Reinforced Tissue Matrix. | OviTex® | TELA BIO, INC. | |
34 | 00810028391833 | 340-00-002 | Arsenal Ankle Hook Plate Guide | TRILLIANT SURGICAL, LLC | ||
35 | 00810028391826 | 340-40-006 | 4.0mm Arsenal Ankle Drill Sleeves | TRILLIANT SURGICAL, LLC | ||
36 | 00810028391819 | 340-35-006 | 3.5mm Arsenal Ankle Drill Sleeves | TRILLIANT SURGICAL, LLC | ||
37 | 00810028391802 | 340-27-006 | 2.7mm Arsenal Ankle Drill Sleeves | TRILLIANT SURGICAL, LLC | ||
38 | 00810028391796 | 340-00-001 | Arsenal Ankle Variable/Static Angle Drill Guide | TRILLIANT SURGICAL, LLC | ||
39 | 00810028391789 | 330-00-022 | Arsenal Drill Tower 3.5mm Insert | TRILLIANT SURGICAL, LLC | ||
40 | 00810028391772 | 330-00-021 | Arsenal Drill Tower 2.7/4.0mm Insert | TRILLIANT SURGICAL, LLC | ||
41 | 00810028391765 | 330-00-020 | Arsenal Drill Tower Outer Sleeve | TRILLIANT SURGICAL, LLC | ||
42 | 00810021865072 | P02 N0101 | TARGETING GUIDE, SCREW | CoLink® NeoFuse | IN2BONES USA, LLC | |
43 | 00810021865065 | P02 N0091 | TARGETING GUIDE, ANTERO-LATERAL, LEFT | CoLink® NeoFuse | IN2BONES USA, LLC | |
44 | 00810021865058 | P02 N0081 | TARGETING GUIDE, ANTERO-LATERAL, RIGHT | CoLink® NeoFuse | IN2BONES USA, LLC | |
45 | 00810021865041 | P02 N0071 | TARGETING GUIDE, ANTERIOR, LEFT | CoLink® NeoFuse | IN2BONES USA, LLC | |
46 | 00810021865034 | P02 N0061 | TARGETING GUIDE, ANTERIOR, RIGHT | CoLink® NeoFuse | IN2BONES USA, LLC | |
47 | 00810021864983 | P02 N0011 | LOCKING DRILL GUIDE, Ø3.2 | CoLink® NeoFuse | IN2BONES USA, LLC | |
48 | 00810021863702 | P04 N0281 | COLINK 2, LOCKING DRILL GUIDE, 2.0 MM | CoLink® 2 | IN2BONES USA, LLC | |
49 | 00810021862248 | P08 N0081 | CALCANEAL SYSTEM LOCKING DRILL GUIDE, Ø2.5 | In2Bones USA | IN2BONES USA, LLC | |
50 | 00810021861401 | P04 N0271 | K-wire, S Trocar, 4x .062 | In2Bones USA | IN2BONES USA, LLC |