No | Primary DI | Version or Model | Catalog Number | Device Description | Product Code | Product Code Name | Device Class | Brand Name |
---|---|---|---|---|---|---|---|---|
1 | 00850268007279 | 1080-547 | iTotal® CR 12mm Tibial Keel Punch Tip Reusable Instrument | JWH | Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer | 2 | iTotal® CR Tibial Keel Punch Tip | |
2 | 00850268007262 | 1080-546 | iTotal® CR 10mm Tibial Keel Punch Tip Reusable Instrument | JWH | Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer | 2 | iTotal® CR Tibial Keel Punch Tip | |
3 | 00850268007255 | 1080-527 | iTotal® CR 14mm Tibial Keel Punch Tip Reusable Instrument | JWH | Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer | 2 | iTotal® CR Tibial Keel Punch Tip | |
4 | 00850268007248 | 1080-526 | iTotal® CR 12mm Tibial Keel Punch Tip Reusable Instrument | JWH | Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer | 2 | iTotal® CR Tibial Keel Punch Tip | |
5 | 00850268007231 | 1080-525 | iTotal® CR 10mm Tibial Keel Punch Tip Reusable Instrument | JWH | Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer | 2 | iTotal® CR Tibial Keel Punch Tip | |
6 | 00850268007200 | 1080-536 | iTotal® CR Tibial Tray Impactor Tip Reusable Instrument | JWH | Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer | 2 | iTotal® CR Tibial Tray Impactor Tip | |
7 | 00810933030674 | 1080-221 | OOG,OIY | Knee Arthroplasty Implantation System,Prosthesis, Knee, Patellofemorotibial, Sem Knee Arthroplasty Implantation System,Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer + Additive/Metal/Polymer + Additive | 2 | ITOTAL IDENTITY LARGE KEEL PUNCH | ||
8 | 00810933031305 | 1080-125 | 1080-125 | Identity Universal Reusable Instrument Lid Trifecta | LXH | Orthopedic Manual Surgical Instrument | 1 | Identity Universal Reusable Instrument Lid Trifecta |
9 | 00810933031237 | 1080-660 | 1080-660 | OrthoGroup Cup Impactor | LXH | Orthopedic Manual Surgical Instrument | 1 | Cordera Hip System OrthoGroup Cup Impactor |
10 | 00810933031121 | 1080-649 | 1080-649 | Femoral Stem Extractor Loop Adaptor | LXH | Orthopedic Manual Surgical Instrument | 1 | Cordera Hip System Femoral Stem Extractor Loop Adaptor |
11 | 00810933031114 | 1080-646 | 1080-646 | Offset Cup Impactor, Enztec | LXH | Orthopedic Manual Surgical Instrument | 1 | Cordera Hip System Offset Cup Impactor, Enztec |
12 | 00810933031107 | 1080-645 | 1080-645 | Offset Reamer Driver, Enztec | LXH | Orthopedic Manual Surgical Instrument | 1 | Cordera Hip System Offset Reamer Driver, Enztec |
13 | M572TPS0101400011 | TPS010140001 | TPS0101400 | ITOTAL IDENTITY PS TIBIAL INSERT, IPOLY, 14MM | JWH,OIY,OOG | Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer,Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer + Additive/Metal/Polymer + Additive,Knee Arthroplasty Implantation System | 2 | Total Identity Posterior Stabilized Knee Replacement System |
14 | M572RPS1011113011 | RPS101111301 | RPS1011113 | N/A | OOG,JWH | Knee Arthroplasty Implantation System,Prosthesis, Knee, Patellofemorotibial, Sem Knee Arthroplasty Implantation System,Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer | 2 | iTotal® PS Tibial Tray Kit |
15 | M572POV0113809011 | POV011380901 | POV0113809 | JWH | Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer | 2 | ITOTAL UHMWPE 38MM X 9MM CEMENTED OVAL PATELLA IMPLANT | |
16 | M572POV0214110011 | POV021411001 | POV0214110 | JWH | Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer | 2 | ITOTAL IPOLY XE 41MM X 10MM CEMENTED OVAL PATELLA IMPLANT | |
17 | M572PAT0114411011 | PAT011441101 | PAT0114411 | JWH | Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer | 2 | ITOTAL-IPOLY-44MM X 11MM CEMENTED PATELLA IMPLANT | |
18 | M572PAT0114110011 | PAT011411001 | PAT0114110 | N/A | JWH | Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer | 2 | iTotal® Patella |
19 | M572PAT0113808011 | PAT011380801 | PAT0113808 | JWH | Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer | 2 | iTotal® Patella | |
20 | M572PAT0113507011 | PAT011350701 | PAT0113507 | N/A | JWH | Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer | 2 | iTotal® Patella |
21 | M572PAT0113206011 | PAT011320601 | PAT0113206 | N/A | JWH | Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer | 2 | iTotal® Patella |
22 | M572PAT0112906011 | PAT011290601 | PAT0112906 | N/A | JWH | Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer | 2 | iTotal® Patella |
23 | M572HES03402CS011 | HES-034-02CS-01 | HES-034-02CS | ACTERA HIP STEM COLLARED SZ 2, STD OFFSET | LPH,LZO,MEH,OQG | Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented,Prosthesis, Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented,Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented Or Non-Porous, Uncemented,Prosthesis, Hip, Semi-Constrained, Uncemented, Metal / Polymer, Non-Porous, Calcium Phosphate,Hip Prosthesis, Semi-Constrained, Cemented, Metal/Polymer, + Additive, Porous, Uncemented | 2 | ACTERA HIP STEM |
24 | M572HES03402CH011 | HES-034-02CH-01 | HES-034-02CH | ACTERA HIP STEM COLLARED SZ 2, HIGH OFFSET | LPH,LZO,OQG,MEH | Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented,Prosthesis, Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented,Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented Or Non-Porous, Uncemented,Hip Prosthesis, Semi-Constrained, Cemented, Metal/Polymer, + Additive, Porous, Uncemented,Prosthesis, Hip, Semi-Constrained, Uncemented, Metal / Polymer, Non-Porous, Calcium Phosphate | 2 | ACTERA HIP STEM |
25 | M5726556C012011 | 6556C01201 | 6556-C-012 | Triathlon AS-1 PS Surgical Instruments, Cementless, PS insert, box ream, sizes Triathlon AS-1 PS Surgical Instruments, Cementless, PS insert, box ream, sizes 0-8, Right and Left | OOG,JWH | Knee Arthroplasty Implantation System,Prosthesis, Knee, Patellofemorotibial, Sem Knee Arthroplasty Implantation System,Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer | 2 | Triathlon AS-1 PS Box Ream Cementless Instrumentation Kit |
26 | M5726556C011011 | 6556C01101 | 6556-C-011 | Triathlon AS-1 PS Surgical Instruments, PS insert, cemented, box ream, sizes 0- Triathlon AS-1 PS Surgical Instruments, PS insert, cemented, box ream, sizes 0-8 Right and Left | OOG,JWH | Knee Arthroplasty Implantation System,Prosthesis, Knee, Patellofemorotibial, Sem Knee Arthroplasty Implantation System,Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer | 2 | Triathlon AS-1 PS Box Ream Cemented Instrumentation Kit |
27 | M5726556C009011 | 6556C00901 | 6556-C-009 | Triathlon AS-1 PS Surgical Instruments, CS insert, cemented, ream, sizes 0-8 Ri Triathlon AS-1 PS Surgical Instruments, CS insert, cemented, ream, sizes 0-8 Right and Left | OOG,JWH | Knee Arthroplasty Implantation System,Prosthesis, Knee, Patellofemorotibial, Sem Knee Arthroplasty Implantation System,Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer | 2 | Triathlon AS-1 PS Ream CS Insert Cemented Instrumentation Kit |
28 | 00810933030681 | 1080-222 | OOG,OIY | Knee Arthroplasty Implantation System,Prosthesis, Knee, Patellofemorotibial, Sem Knee Arthroplasty Implantation System,Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer + Additive/Metal/Polymer + Additive | 2 | ITOTAL IDENTITY ALIGNMENT ROD | ||
29 | 00850268007286 | 1080-548 | iTotal® CR 14mm Tibial Keel Punch Tip Reusable Instrument | JWH | Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer | 2 | iTotal® CR Keel Punch Tip | |
30 | 00810933030643 | 1080-218 | OOG,OIY | Knee Arthroplasty Implantation System,Prosthesis, Knee, Patellofemorotibial, Sem Knee Arthroplasty Implantation System,Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer + Additive/Metal/Polymer + Additive | 2 | ITOTAL IDENTITY ROUND PATELLA HEAD SIZER 38-41-44MM | ||
31 | 00810933031251 | 1080-121 | 1080-121 | Acetabular Reusable Instrument Tray, insert and base | LXH | Orthopedic Manual Surgical Instrument | 1 | Cordera Hip System Acetabular Reusable Instrument Tray, insert and base |
32 | 00810933031152 | 1080-652 | 1080-652 | (Stainless Steel) Trial Neck 132degree,29.0mm | LPH | Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented | 2 | Cordera Hip System (Stainless Steel) Trial Neck 132degree,29.0mm |
33 | 00810933031145 | 1080-651 | 1080-651 | (Stainless Steel)Trial Neck 127degree, 29.0mm | LPH | Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented | 2 | Cordera Hip System (Stainless Steel) Trial Neck 127degree, 29.0mm |
34 | 00810933031138 | 1080-650 | 1080-650 | Femoral Stem Extractor Handle Extension | LXH | Orthopedic Manual Surgical Instrument | 1 | Cordera Hip System Femoral Stem Extractor Handle Extension |
35 | 00810933031091 | 1080-648 | 1080-648 | Femoral Stem Extractor Straight Adaptor, Threaded | LXH | Orthopedic Manual Surgical Instrument | 1 | Cordera Hip System Femoral Stem Extractor Straight Adaptor, Threaded |
36 | 00810933030582 | 1080-212 | OOG,OIY | Knee Arthroplasty Implantation System,Prosthesis, Knee, Patellofemorotibial, Sem Knee Arthroplasty Implantation System,Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer + Additive/Metal/Polymer + Additive | 2 | ITOTAL IDENTITY IMPACTOR HANDLE | ||
37 | 00810933030537 | 1080-226 | OOG,OIY | Knee Arthroplasty Implantation System,Prosthesis, Knee, Patellofemorotibial, Sem Knee Arthroplasty Implantation System,Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer + Additive/Metal/Polymer + Additive | 2 | ITOTAL IDENTITY TIBIAL CUT GUIDE SMALL RIGHT | ||
38 | 00810933030520 | 1080-225 | OOG,OIY | Knee Arthroplasty Implantation System,Prosthesis, Knee, Patellofemorotibial, Sem Knee Arthroplasty Implantation System,Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer + Additive/Metal/Polymer + Additive | 2 | ITOTAL IDENTITY TIBIAL CUT GUIDE SMALL LEFT | ||
39 | 00810933030506 | 1080-223 | OOG,OIY | Knee Arthroplasty Implantation System,Prosthesis, Knee, Patellofemorotibial, Sem Knee Arthroplasty Implantation System,Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer + Additive/Metal/Polymer + Additive | 2 | ITOTAL IDENTITY FEMORAL CUT GUIDE SMALL | ||
40 | 00810933030483 | 1080-210 | OOG,OIY | Knee Arthroplasty Implantation System,Prosthesis, Knee, Patellofemorotibial, Sem Knee Arthroplasty Implantation System,Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer + Additive/Metal/Polymer + Additive | 2 | ITOTAL IDENTITY EXTENSION WRENCH HANDLE | ||
41 | 00810933030452 | 1080-206 | OOG,OIY | Knee Arthroplasty Implantation System,Prosthesis, Knee, Patellofemorotibial, Sem Knee Arthroplasty Implantation System,Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer + Additive/Metal/Polymer + Additive | 2 | ITOTAL OVAL PATELLA TRIAL 44MM | ||
42 | 00810933030391 | 1080-229 | OOG,OIY | Knee Arthroplasty Implantation System,Prosthesis, Knee, Patellofemorotibial, Sem Knee Arthroplasty Implantation System,Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer + Additive/Metal/Polymer + Additive | 2 | ITOTAL PATELLA TRIAL 44MM ROUND DOME | ||
43 | M572PAT0214110011 | PAT021411001 | PAT0214110 | N/A | OIY | Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer + Add Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer + Additive/Metal/Polymer + Additive | 2 | iTotal® iPoly XE™ Patella |
44 | M572TCR3011113011 | TCR301111301 | TCR3011113 | ITOTAL IDENTITY CR TIBIAL TRAY (TITANIUM, CEMENTED) | OOG,JWH,OIY | Knee Arthroplasty Implantation System,Prosthesis, Knee, Patellofemorotibial, Sem Knee Arthroplasty Implantation System,Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer,Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer + Additive/Metal/Polymer + Additive | 2 | iTotal® Identity Cruciate Retaining Knee Replacement System |
45 | M572TCR1011112011 | TCR101111201 | TCR1011112 | ITOTAL IDENTITY CR FEMORAL IMPLANT (COCR, CEMENTED) | OIY,OOG,JWH | Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer + Add Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer + Additive/Metal/Polymer + Additive,Knee Arthroplasty Implantation System,Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer | 2 | iTotal® Identity Cruciate Retaining Knee Replacement System |
46 | M572PAT0213808011 | PAT021380801 | PAT0213808 | N/A | OIY,JWH | Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer + Add Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer + Additive/Metal/Polymer + Additive,Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer | 2 | iTotal® iPoly XE™ Patella |
47 | M572TCR020140J011 | TCR020140J01 | TCR020140J | ITOTAL IDENTITY CR TIBIAL INSERT, IPOLY XE, SINGLE, 14MM | OIY,OOG,JWH | Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer + Add Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer + Additive/Metal/Polymer + Additive,Knee Arthroplasty Implantation System,Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer | 2 | iTotal® Identity Cruciate Retaining Knee Replacement System |
48 | M572TCR0201400011 | TCR020140001 | TCR0201400 | ITOTAL IDENTITY CR TIBIAL INSERT, IPOLY XE, MEDIAL, 14MM | OIY,OOG,JWH | Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer + Add Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer + Additive/Metal/Polymer + Additive,Knee Arthroplasty Implantation System,Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer | 2 | iTotal® Identity Cruciate Retaining Knee Replacement System |
49 | M572TCR020130H011 | TCR020130H01 | TCR020130H | ITOTAL IDENTITY CR TIBIAL INSERT, IPOLY XE, SINGLE, 13MM | OIY,OOG,JWH | Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer + Add Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer + Additive/Metal/Polymer + Additive,Knee Arthroplasty Implantation System,Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer | 2 | iTotal® Identity Cruciate Retaining Knee Replacement System |
50 | M572TCR0201300011 | TCR020130001 | TCR0201300 | ITOTAL IDENTITY CR TIBIAL INSERT, IPOLY XE, MEDIAL, 13MM | OIY,OOG,JWH | Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer + Add Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer + Additive/Metal/Polymer + Additive,Knee Arthroplasty Implantation System,Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer | 2 | iTotal® Identity Cruciate Retaining Knee Replacement System |
No | Primary DI | Version or Model | Catalog Number | Device Description | Brand Name | Organization Name |
---|---|---|---|---|---|---|
1 | 00810482031009 | 9014-CTL7 | 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 trials are available in parallel and lordotic configurations, 14mmX11mm and 17mmX13mm sizes and thicknesses between 5mm and 11mm. | Blustone Synergy Cervical Trial (Slate) | BLUSTONE SYNERGY, LLC | |
2 | 00810482031375 | 9017-CTP09 | 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 trials are available in 11mmX14mm and 13mmX17mm footprints, lordotic and parallel configurations, and thicknesses from 5mm to 11mm. | Blustone Synergy Cervical Trial (Slate) | BLUSTONE SYNERGY, LLC | |
3 | 00810482031368 | 9017-CTP08 | 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 trials are available in 11mmX14mm and 13mmX17mm footprints, lordotic and parallel configurations, and thicknesses from 5mm to 11mm. | Blustone Synergy Cervical Trial (Slate) | BLUSTONE SYNERGY, LLC | |
4 | 00810482031351 | 9017-CTP07 | 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 trials are available in 11mmX14mm and 13mmX17mm footprints, lordotic and parallel configurations, and thicknesses from 5mm to 11mm. | Blustone Synergy Cervical Trial (Slate) | BLUSTONE SYNERGY, LLC | |
5 | 00810482031344 | 9017-CTP06 | 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 trials are available in 11mmX14mm and 13mmX17mm footprints, lordotic and parallel configurations, and thicknesses from 5mm to 11mm. | Blustone Synergy Cervical Trial (Slate) | BLUSTONE SYNERGY, LLC | |
6 | 00810482031337 | 9017-CTP05 | 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 trials are available in 11mmX14mm and 13mmX17mm footprints, lordotic and parallel configurations, and thicknesses from 5mm to 11mm. | Blustone Synergy Cervical Trial (Slate) | BLUSTONE SYNERGY, LLC | |
7 | 00810482031320 | 9017-CTP11 | 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 trials are available in 11mmX14mm and 13mmX17mm footprints, lordotic and parallel configurations, and thicknesses from 5mm to 11mm. | Blustone Synergy Cervical Trial (Slate) | BLUSTONE SYNERGY, LLC | |
8 | 00810482031313 | 9017-CTP10 | 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 trials are available in 11mmX14mm and 13mmX17mm footprints, lordotic and parallel configurations, and thicknesses from 5mm to 11mm. | Blustone Synergy Cervical Trial (Slate) | BLUSTONE SYNERGY, LLC | |
9 | 00810482031306 | 9017-CTL10 | 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 trials are available in 11mmX14mm and 13mmX17mm footprints, lordotic and parallel configurations, and thicknesses from 5mm to 11mm. | Blustone Synergy Cervical Trial (Slate) | BLUSTONE SYNERGY, LLC | |
10 | 00810482031290 | 9017-CTL09 | 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 trials are available in 11mmX14mm and 13mmX17mm footprints, lordotic and parallel configurations, and thicknesses from 5mm to 11mm. | Blustone Synergy Cervical Trial (Slate) | BLUSTONE SYNERGY, LLC | |
11 | 00810482031283 | 9017-CTL08 | 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 trials are available in 11mmX14mm and 13mmX17mm footprints, lordotic and parallel configurations, and thicknesses from 5mm to 11mm. | Blustone Synergy Cervical Trial (Slate) | BLUSTONE SYNERGY, LLC | |
12 | 00810482031276 | 9017-CTL07 | 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 trials are available in 11mmX14mm and 13mmX17mm footprints, lordotic and parallel configurations, and thicknesses from 5mm to 11mm. | Blustone Synergy Cervical Trial (Slate) | BLUSTONE SYNERGY, LLC | |
13 | 00810482031269 | 9017-CTL06 | 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 trials are available in 11mmX14mm and 13mmX17mm footprints, lordotic and parallel configurations, and thicknesses from 5mm to 11mm. | Blustone Synergy Cervical Trial (Slate) | BLUSTONE SYNERGY, LLC | |
14 | 00810482031252 | 9017-CTL05 | 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 trials are available in 11mmX14mm and 13mmX17mm footprints, lordotic and parallel configurations, and thicknesses from 5mm to 11mm. | Blustone Synergy Cervical Trial (Slate) | BLUSTONE SYNERGY, LLC | |
15 | 00810482031245 | 9017-CTL11 | 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 trials are available in 11mmX14mm and 13mmX17mm footprints, lordotic and parallel configurations, and thicknesses from 5mm to 11mm. | Blustone Synergy Cervical Trial (Slate) | BLUSTONE SYNERGY, LLC | |
16 | 00810482031092 | 9014-CTP9 | 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 trials are available in parallel and lordotic configurations, 14mmX11mm and 17mmX13mm sizes and thicknesses between 5mm and 11mm. | Blustone Synergy Cervical Trial (Slate) | BLUSTONE SYNERGY, LLC | |
17 | 00810482031085 | 9014-CTP8 | 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 trials are available in parallel and lordotic configurations, 14mmX11mm and 17mmX13mm sizes and thicknesses between 5mm and 11mm. | Blustone Synergy Cervical Trial (Slate) | BLUSTONE SYNERGY, LLC | |
18 | 00810482031078 | 9014-CTP7 | 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 trials are available in parallel and lordotic configurations, 14mmX11mm and 17mmX13mm sizes and thicknesses between 5mm and 11mm. | Blustone Synergy Cervical Trial (Slate) | BLUSTONE SYNERGY, LLC | |
19 | 00810482031061 | 9014-CTP6 | 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 trials are available in parallel and lordotic configurations, 14mmX11mm and 17mmX13mm sizes and thicknesses between 5mm and 11mm. | Blustone Synergy Cervical Trial (Slate) | BLUSTONE SYNERGY, LLC | |
20 | 00810482031054 | 9014-CTP5 | 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 trials are available in parallel and lordotic configurations, 14mmX11mm and 17mmX13mm sizes and thicknesses between 5mm and 11mm. | Blustone Synergy Cervical Trial (Slate) | BLUSTONE SYNERGY, LLC | |
21 | 00810482031047 | 9014-CTP11 | 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 trials are available in parallel and lordotic configurations, 14mmX11mm and 17mmX13mm sizes and thicknesses between 5mm and 11mm. | Blustone Synergy Cervical Trial (Slate) | BLUSTONE SYNERGY, LLC | |
22 | 00810482031030 | 9014-CTP10 | 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 trials are available in parallel and lordotic configurations, 14mmX11mm and 17mmX13mm sizes and thicknesses between 5mm and 11mm. | Blustone Synergy Cervical Trial (Slate) | BLUSTONE SYNERGY, LLC | |
23 | 00810482030996 | 9014-CTL6 | 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 trials are available in parallel and lordotic configurations, 14mmX11mm and 17mmX13mm sizes and thicknesses between 5mm and 11mm. | Blustone Synergy Cervical Trial (Slate) | BLUSTONE SYNERGY, LLC | |
24 | 00810482030989 | 9014-CTL5 | 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 trials are available in parallel and lordotic configurations, 14mmX11mm and 17mmX13mm sizes and thicknesses between 5mm and 11mm. | Blustone Synergy Cervical Trial (Slate) | BLUSTONE SYNERGY, LLC | |
25 | 00810482030972 | 9014-CTL11 | 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 trials are available in parallel and lordotic configurations, 14mmX11mm and 17mmX13mm sizes and thicknesses between 5mm and 11mm. | Blustone Synergy Cervical Trial (Slate) | BLUSTONE SYNERGY, LLC | |
26 | 00810482030965 | 9014-CTL10 | 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 trials are available in parallel and lordotic configurations, 14mmX11mm and 17mmX13mm sizes and thicknesses between 5mm and 11mm. | Blustone Synergy Cervical Trial (Slate) | BLUSTONE SYNERGY, LLC | |
27 | 00810482030767 | 9000-SP15 | The Blustone Synergy Lumbar Interbody Fusion System is implanted using a combina The Blustone Synergy Lumbar 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 lumbar trials/spreaders are available in sizes between 7mm and 15mm. | Blustone Synergy Lumbar Trial/Spreader (Basalt, Obsidian, Magma) | BLUSTONE SYNERGY, LLC | |
28 | 00810482030750 | 9000-SP14 | The Blustone Synergy Lumbar Interbody Fusion System is implanted using a combina The Blustone Synergy Lumbar 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 lumbar trials/spreaders are available in sizes between 7mm and 15mm. | Blustone Synergy Lumbar Trial/Spreader (Basalt, Obsidian, Magma) | BLUSTONE SYNERGY, LLC | |
29 | 00810482030743 | 9000-SP13 | The Blustone Synergy Lumbar Interbody Fusion System is implanted using a combina The Blustone Synergy Lumbar 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 lumbar trials/spreaders are available in sizes between 7mm and 15mm. | Blustone Synergy Lumbar Trial/Spreader (Basalt, Obsidian, Magma) | BLUSTONE SYNERGY, LLC | |
30 | 00810482030736 | 9000-SP12 | The Blustone Synergy Lumbar Interbody Fusion System is implanted using a combina The Blustone Synergy Lumbar 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 lumbar trials/spreaders are available in sizes between 7mm and 15mm. | Blustone Synergy Lumbar Trial/Spreader (Basalt, Obsidian, Magma) | BLUSTONE SYNERGY, LLC | |
31 | 00810482030729 | 9000-SP11 | The Blustone Synergy Lumbar Interbody Fusion System is implanted using a combina The Blustone Synergy Lumbar 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 lumbar trials/spreaders are available in sizes between 7mm and 15mm. | Blustone Synergy Lumbar Trial/Spreader (Basalt, Obsidian, Magma) | BLUSTONE SYNERGY, LLC | |
32 | 00810482030712 | 9000-SP10 | The Blustone Synergy Lumbar Interbody Fusion System is implanted using a combina The Blustone Synergy Lumbar 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 lumbar trials/spreaders are available in sizes between 7mm and 15mm. | Blustone Synergy Lumbar Trial/Spreader (Basalt, Obsidian, Magma) | BLUSTONE SYNERGY, LLC | |
33 | 00810482030705 | 9000-SP09 | The Blustone Synergy Lumbar Interbody Fusion System is implanted using a combina The Blustone Synergy Lumbar 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 lumbar trials/spreaders are available in sizes between 7mm and 15mm. | Blustone Synergy Lumbar Trial/Spreader (Basalt, Obsidian, Magma) | BLUSTONE SYNERGY, LLC | |
34 | 00810482030699 | 9000-SP08 | The Blustone Synergy Lumbar Interbody Fusion System is implanted using a combina The Blustone Synergy Lumbar 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 lumbar trials/spreaders are available in sizes between 7mm and 15mm. | Blustone Synergy Lumbar Trial/Spreader (Basalt, Obsidian, Magma) | BLUSTONE SYNERGY, LLC | |
35 | 00810482030675 | 9000-SP07 | The Blustone Synergy Lumbar Interbody Fusion System is implanted using a combina The Blustone Synergy Lumbar 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 lumbar trials/spreaders are available in sizes between 7mm and 15mm. | Blustone Synergy Lumbar Trial/Spreader (Basalt, Obsidian, Magma) | BLUSTONE SYNERGY, LLC | |
36 | 00810074751131 | LSTS-SM0614-SH | LSTS-SM0614-SH | 4WEB Medical | 4WEB MEDICAL | |
37 | 00810074751124 | LSTS-SM0612-SH | LSTS-SM0612-SH | 4WEB Medical | 4WEB MEDICAL | |
38 | 00810074751117 | LSTS-SM0610-SH | LSTS-SM0610-SH | 4WEB Medical | 4WEB MEDICAL | |
39 | 00810074751100 | LSTS-SM0608-SH | LSTS-SM0608-SH | 4WEB Medical | 4WEB MEDICAL | |
40 | 00810074755221 | CSTS-00-SM0705-S | CSTS-00-SM0705-S | 4WEB Medical | 4WEB MEDICAL | |
41 | 00810074753319 | CSTS-SA-MDYY10-RS | CSTS-SA-MDYY10-RS | 4WEB Medical | 4WEB MEDICAL | |
42 | 00810074753296 | CSTS-SA-MDYY09-RS | CSTS-SA-MDYY09-RS | 4WEB Medical | 4WEB MEDICAL | |
43 | 00810074753289 | CSTS-SA-MDYY08-RS | CSTS-SA-MDYY08-RS | 4WEB Medical | 4WEB MEDICAL | |
44 | 00810074753272 | CSTS-SA-MDYY07-RS | CSTS-SA-MDYY07-RS | 4WEB Medical | 4WEB MEDICAL | |
45 | 00810074753265 | CSTS-SA-MDYY06-RS | CSTS-SA-MDYY06-RS | 4WEB Medical | 4WEB MEDICAL | |
46 | 00810074753258 | CSTS-SA-MDYY05-RS | CSTS-SA-MDYY05-RS | 4WEB Medical | 4WEB MEDICAL | |
47 | 00810074753227 | CSTS-SA-SMYY10-RS | CSTS-SA-SMYY10-RS | 4WEB Medical | 4WEB MEDICAL | |
48 | 00810074753210 | CSTS-SA-SMYY09-RS | CSTS-SA-SMYY09-RS | 4WEB Medical | 4WEB MEDICAL | |
49 | 00810074753203 | CSTS-SA-SMYY08-RS | CSTS-SA-SMYY08-RS | 4WEB Medical | 4WEB MEDICAL | |
50 | 00810074753197 | CSTS-SA-SMYY07-RS | CSTS-SA-SMYY07-RS | 4WEB Medical | 4WEB MEDICAL |