Other products from "BIOMET ORTHOPEDICS, LLC"
No Primary DI Version or Model Catalog Number Device Description Product Code Product Code Name Device Class Brand Name
1 00887868041464 8153-41-055 815341055 KTT,HTN,HWC,HRS,HTY,JDW,HSB,LXT APPLIANCE, FIXATION, NAIL/BLADE/PLATE COMBINATION, MULTIPLE COMPONENT,WASHER, BO APPLIANCE, FIXATION, NAIL/BLADE/PLATE COMBINATION, MULTIPLE COMPONENT,WASHER, BOLT NUT,Screw, fixation, bone,PLATE, FIXATION, BONE,PIN, FIXATION, SMOOTH,PIN, FIXATION, THREADED,ROD, FIXATION, INTRAMEDULLARY AND ACCESSORIES,APPLIANCE, FIXATION, NAIL/BLADE/PLATE COMBINATION, MULTIPLE COMPONENT, METAL COMPOSITE 2 SCREW, CANCELLOUS
2 00887868041457 8153-41-050 815341050 KTT,JDW,HTN,HWC,LXT,HTY,HSB,HRS APPLIANCE, FIXATION, NAIL/BLADE/PLATE COMBINATION, MULTIPLE COMPONENT,PIN, FIXAT APPLIANCE, FIXATION, NAIL/BLADE/PLATE COMBINATION, MULTIPLE COMPONENT,PIN, FIXATION, THREADED,WASHER, BOLT NUT,Screw, fixation, bone,APPLIANCE, FIXATION, NAIL/BLADE/PLATE COMBINATION, MULTIPLE COMPONENT, METAL COMPOSITE,PIN, FIXATION, SMOOTH,ROD, FIXATION, INTRAMEDULLARY AND ACCESSORIES,PLATE, FIXATION, BONE 2 SCREW, CANCELLOUS
3 00887868041440 8153-41-048 815341048 HTN,HSB,HTY,LXT,JDW,HWC,HRS,KTT WASHER, BOLT NUT,ROD, FIXATION, INTRAMEDULLARY AND ACCESSORIES,PIN, FIXATION, SM WASHER, BOLT NUT,ROD, FIXATION, INTRAMEDULLARY AND ACCESSORIES,PIN, FIXATION, SMOOTH,APPLIANCE, FIXATION, NAIL/BLADE/PLATE COMBINATION, MULTIPLE COMPONENT, METAL COMPOSITE,PIN, FIXATION, THREADED,Screw, fixation, bone,PLATE, FIXATION, BONE,APPLIANCE, FIXATION, NAIL/BLADE/PLATE COMBINATION, MULTIPLE COMPONENT 2 SCREW, CANCELLOUS
4 00887868041433 8153-41-046 815341046 HTN,HTY,KTT,HWC,HSB,JDW,HRS,LXT WASHER, BOLT NUT,PIN, FIXATION, SMOOTH,APPLIANCE, FIXATION, NAIL/BLADE/PLATE COM WASHER, BOLT NUT,PIN, FIXATION, SMOOTH,APPLIANCE, FIXATION, NAIL/BLADE/PLATE COMBINATION, MULTIPLE COMPONENT,Screw, fixation, bone,ROD, FIXATION, INTRAMEDULLARY AND ACCESSORIES,PIN, FIXATION, THREADED,PLATE, FIXATION, BONE,APPLIANCE, FIXATION, NAIL/BLADE/PLATE COMBINATION, MULTIPLE COMPONENT, METAL COMPOSITE 2 SCREW, CANCELLOUS
5 00887868041426 8153-41-044 815341044 LXT,HTN,HSB,HWC,HTY,KTT,JDW,HRS APPLIANCE, FIXATION, NAIL/BLADE/PLATE COMBINATION, MULTIPLE COMPONENT, METAL COM APPLIANCE, FIXATION, NAIL/BLADE/PLATE COMBINATION, MULTIPLE COMPONENT, METAL COMPOSITE,WASHER, BOLT NUT,ROD, FIXATION, INTRAMEDULLARY AND ACCESSORIES,Screw, fixation, bone,PIN, FIXATION, SMOOTH,APPLIANCE, FIXATION, NAIL/BLADE/PLATE COMBINATION, MULTIPLE COMPONENT,PIN, FIXATION, THREADED,PLATE, FIXATION, BONE 2 SCREW, CANCELLOUS
6 00887868041419 8153-41-042 815341042 HTN,LXT,JDW,HRS,HSB,HWC,HTY,KTT WASHER, BOLT NUT,APPLIANCE, FIXATION, NAIL/BLADE/PLATE COMBINATION, MULTIPLE COM WASHER, BOLT NUT,APPLIANCE, FIXATION, NAIL/BLADE/PLATE COMBINATION, MULTIPLE COMPONENT, METAL COMPOSITE,PIN, FIXATION, THREADED,PLATE, FIXATION, BONE,ROD, FIXATION, INTRAMEDULLARY AND ACCESSORIES,Screw, fixation, bone,PIN, FIXATION, SMOOTH,APPLIANCE, FIXATION, NAIL/BLADE/PLATE COMBINATION, MULTIPLE COMPONENT 2 SCREW, CANCELLOUS
7 00887868041402 8153-41-040 815341040 KTT,HWC,HSB,HRS,JDW,HTY,HTN,LXT APPLIANCE, FIXATION, NAIL/BLADE/PLATE COMBINATION, MULTIPLE COMPONENT,Screw, fix APPLIANCE, FIXATION, NAIL/BLADE/PLATE COMBINATION, MULTIPLE COMPONENT,Screw, fixation, bone,ROD, FIXATION, INTRAMEDULLARY AND ACCESSORIES,PLATE, FIXATION, BONE,PIN, FIXATION, THREADED,PIN, FIXATION, SMOOTH,WASHER, BOLT NUT,APPLIANCE, FIXATION, NAIL/BLADE/PLATE COMBINATION, MULTIPLE COMPONENT, METAL COMPOSITE 2 SCREW, CANCELLOUS
8 00887868041396 8153-41-038 815341038 HSB,HTY,HTN,LXT,KTT,HWC,JDW,HRS ROD, FIXATION, INTRAMEDULLARY AND ACCESSORIES,PIN, FIXATION, SMOOTH,WASHER, BOLT ROD, FIXATION, INTRAMEDULLARY AND ACCESSORIES,PIN, FIXATION, SMOOTH,WASHER, BOLT NUT,APPLIANCE, FIXATION, NAIL/BLADE/PLATE COMBINATION, MULTIPLE COMPONENT, METAL COMPOSITE,APPLIANCE, FIXATION, NAIL/BLADE/PLATE COMBINATION, MULTIPLE COMPONENT,Screw, fixation, bone,PIN, FIXATION, THREADED,PLATE, FIXATION, BONE 2 SCREW, CANCELLOUS
9 00887868041389 8153-41-036 815341036 KTT,HRS,JDW,HSB,LXT,HTY,HTN,HWC APPLIANCE, FIXATION, NAIL/BLADE/PLATE COMBINATION, MULTIPLE COMPONENT,PLATE, FIX APPLIANCE, FIXATION, NAIL/BLADE/PLATE COMBINATION, MULTIPLE COMPONENT,PLATE, FIXATION, BONE,PIN, FIXATION, THREADED,ROD, FIXATION, INTRAMEDULLARY AND ACCESSORIES,APPLIANCE, FIXATION, NAIL/BLADE/PLATE COMBINATION, MULTIPLE COMPONENT, METAL COMPOSITE,PIN, FIXATION, SMOOTH,WASHER, BOLT NUT,Screw, fixation, bone 2 SCREW, CANCELLOUS
10 00887868041372 8153-41-034 815341034 HSB,KTT,JDW,HTY,HWC,LXT,HRS,HTN ROD, FIXATION, INTRAMEDULLARY AND ACCESSORIES,APPLIANCE, FIXATION, NAIL/BLADE/PL ROD, FIXATION, INTRAMEDULLARY AND ACCESSORIES,APPLIANCE, FIXATION, NAIL/BLADE/PLATE COMBINATION, MULTIPLE COMPONENT,PIN, FIXATION, THREADED,PIN, FIXATION, SMOOTH,Screw, fixation, bone,APPLIANCE, FIXATION, NAIL/BLADE/PLATE COMBINATION, MULTIPLE COMPONENT, METAL COMPOSITE,PLATE, FIXATION, BONE,WASHER, BOLT NUT 2 SCREW, CANCELLOUS
11 00887868041365 8153-41-032 815341032 HRS,KTT,HTY,JDW,LXT,HWC,HTN,HSB PLATE, FIXATION, BONE,APPLIANCE, FIXATION, NAIL/BLADE/PLATE COMBINATION, MULTIPL PLATE, FIXATION, BONE,APPLIANCE, FIXATION, NAIL/BLADE/PLATE COMBINATION, MULTIPLE COMPONENT,PIN, FIXATION, SMOOTH,PIN, FIXATION, THREADED,APPLIANCE, FIXATION, NAIL/BLADE/PLATE COMBINATION, MULTIPLE COMPONENT, METAL COMPOSITE,Screw, fixation, bone,WASHER, BOLT NUT,ROD, FIXATION, INTRAMEDULLARY AND ACCESSORIES 2 SCREW, CANCELLOUS
12 00887868041358 8153-41-030 815341030 LXT,JDW,HWC,HTN,HRS,HSB,KTT,HTY APPLIANCE, FIXATION, NAIL/BLADE/PLATE COMBINATION, MULTIPLE COMPONENT, METAL COM APPLIANCE, FIXATION, NAIL/BLADE/PLATE COMBINATION, MULTIPLE COMPONENT, METAL COMPOSITE,PIN, FIXATION, THREADED,Screw, fixation, bone,WASHER, BOLT NUT,PLATE, FIXATION, BONE,ROD, FIXATION, INTRAMEDULLARY AND ACCESSORIES,APPLIANCE, FIXATION, NAIL/BLADE/PLATE COMBINATION, MULTIPLE COMPONENT,PIN, FIXATION, SMOOTH 2 SCREW, CANCELLOUS
13 00887868041341 8153-41-028 815341028 LXT,KTT,HTN,HWC,HSB,JDW,HTY,HRS APPLIANCE, FIXATION, NAIL/BLADE/PLATE COMBINATION, MULTIPLE COMPONENT, METAL COM APPLIANCE, FIXATION, NAIL/BLADE/PLATE COMBINATION, MULTIPLE COMPONENT, METAL COMPOSITE,APPLIANCE, FIXATION, NAIL/BLADE/PLATE COMBINATION, MULTIPLE COMPONENT,WASHER, BOLT NUT,Screw, fixation, bone,ROD, FIXATION, INTRAMEDULLARY AND ACCESSORIES,PIN, FIXATION, THREADED,PIN, FIXATION, SMOOTH,PLATE, FIXATION, BONE 2 SCREW, CANCELLOUS
14 00887868041334 8153-41-026 815341026 LXT,HSB,HTN,JDW,HWC,HRS,KTT,HTY APPLIANCE, FIXATION, NAIL/BLADE/PLATE COMBINATION, MULTIPLE COMPONENT, METAL COM APPLIANCE, FIXATION, NAIL/BLADE/PLATE COMBINATION, MULTIPLE COMPONENT, METAL COMPOSITE,ROD, FIXATION, INTRAMEDULLARY AND ACCESSORIES,WASHER, BOLT NUT,PIN, FIXATION, THREADED,Screw, fixation, bone,PLATE, FIXATION, BONE,APPLIANCE, FIXATION, NAIL/BLADE/PLATE COMBINATION, MULTIPLE COMPONENT,PIN, FIXATION, SMOOTH 2 SCREW, CANCELLOUS
15 00887868041327 8153-41-024 815341024 HRS,HWC,LXT,KTT,JDW,HTN,HTY,HSB PLATE, FIXATION, BONE,Screw, fixation, bone,APPLIANCE, FIXATION, NAIL/BLADE/PLAT PLATE, FIXATION, BONE,Screw, fixation, bone,APPLIANCE, FIXATION, NAIL/BLADE/PLATE COMBINATION, MULTIPLE COMPONENT, METAL COMPOSITE,APPLIANCE, FIXATION, NAIL/BLADE/PLATE COMBINATION, MULTIPLE COMPONENT,PIN, FIXATION, THREADED,WASHER, BOLT NUT,PIN, FIXATION, SMOOTH,ROD, FIXATION, INTRAMEDULLARY AND ACCESSORIES 2 SCREW, CANCELLOUS
16 00887868041310 8153-41-022 815341022 HWC,HTY,LXT,HTN,HSB,KTT,JDW,HRS Screw, fixation, bone,PIN, FIXATION, SMOOTH,APPLIANCE, FIXATION, NAIL/BLADE/PLAT Screw, fixation, bone,PIN, FIXATION, SMOOTH,APPLIANCE, FIXATION, NAIL/BLADE/PLATE COMBINATION, MULTIPLE COMPONENT, METAL COMPOSITE,WASHER, BOLT NUT,ROD, FIXATION, INTRAMEDULLARY AND ACCESSORIES,APPLIANCE, FIXATION, NAIL/BLADE/PLATE COMBINATION, MULTIPLE COMPONENT,PIN, FIXATION, THREADED,PLATE, FIXATION, BONE 2 SCREW, CANCELLOUS
17 00887868041303 8153-41-020 815341020 HTY,HWC,HTN,JDW,HSB,LXT,KTT,HRS PIN, FIXATION, SMOOTH,Screw, fixation, bone,WASHER, BOLT NUT,PIN, FIXATION, THRE PIN, FIXATION, SMOOTH,Screw, fixation, bone,WASHER, BOLT NUT,PIN, FIXATION, THREADED,ROD, FIXATION, INTRAMEDULLARY AND ACCESSORIES,APPLIANCE, FIXATION, NAIL/BLADE/PLATE COMBINATION, MULTIPLE COMPONENT, METAL COMPOSITE,APPLIANCE, FIXATION, NAIL/BLADE/PLATE COMBINATION, MULTIPLE COMPONENT,PLATE, FIXATION, BONE 2 SCREW, CANCELLOUS
18 00887868041297 8153-41-018 815341018 LXT,HRS,HTN,KTT,HWC,HTY,JDW,HSB APPLIANCE, FIXATION, NAIL/BLADE/PLATE COMBINATION, MULTIPLE COMPONENT, METAL COM APPLIANCE, FIXATION, NAIL/BLADE/PLATE COMBINATION, MULTIPLE COMPONENT, METAL COMPOSITE,PLATE, FIXATION, BONE,WASHER, BOLT NUT,APPLIANCE, FIXATION, NAIL/BLADE/PLATE COMBINATION, MULTIPLE COMPONENT,Screw, fixation, bone,PIN, FIXATION, SMOOTH,PIN, FIXATION, THREADED,ROD, FIXATION, INTRAMEDULLARY AND ACCESSORIES 2 SCREW, CANCELLOUS
19 00887868041280 8153-41-016 815341016 LXT,HTY,HSB,JDW,HWC,HRS,KTT,HTN APPLIANCE, FIXATION, NAIL/BLADE/PLATE COMBINATION, MULTIPLE COMPONENT, METAL COM APPLIANCE, FIXATION, NAIL/BLADE/PLATE COMBINATION, MULTIPLE COMPONENT, METAL COMPOSITE,PIN, FIXATION, SMOOTH,ROD, FIXATION, INTRAMEDULLARY AND ACCESSORIES,PIN, FIXATION, THREADED,Screw, fixation, bone,PLATE, FIXATION, BONE,APPLIANCE, FIXATION, NAIL/BLADE/PLATE COMBINATION, MULTIPLE COMPONENT,WASHER, BOLT NUT 2 SCREW, CANCELLOUS
20 00887868041273 8153-41-014 815341014 HWC,HSB,HRS,KTT,JDW,HTY,HTN,LXT Screw, fixation, bone,ROD, FIXATION, INTRAMEDULLARY AND ACCESSORIES,PLATE, FIXAT Screw, fixation, bone,ROD, FIXATION, INTRAMEDULLARY AND ACCESSORIES,PLATE, FIXATION, BONE,APPLIANCE, FIXATION, NAIL/BLADE/PLATE COMBINATION, MULTIPLE COMPONENT,PIN, FIXATION, THREADED,PIN, FIXATION, SMOOTH,WASHER, BOLT NUT,APPLIANCE, FIXATION, NAIL/BLADE/PLATE COMBINATION, MULTIPLE COMPONENT, METAL COMPOSITE 2 SCREW, CANCELLOUS
21 00887868041266 8153-41-012 815341012 LXT,HRS,HTN,HTY,HWC,JDW,KTT,HSB APPLIANCE, FIXATION, NAIL/BLADE/PLATE COMBINATION, MULTIPLE COMPONENT, METAL COM APPLIANCE, FIXATION, NAIL/BLADE/PLATE COMBINATION, MULTIPLE COMPONENT, METAL COMPOSITE,PLATE, FIXATION, BONE,WASHER, BOLT NUT,PIN, FIXATION, SMOOTH,Screw, fixation, bone,PIN, FIXATION, THREADED,APPLIANCE, FIXATION, NAIL/BLADE/PLATE COMBINATION, MULTIPLE COMPONENT,ROD, FIXATION, INTRAMEDULLARY AND ACCESSORIES 2 SCREW, CANCELLOUS
22 00887868041259 8153-41-010 815341010 HTN,LXT,HTY,HSB,KTT,JDW,HRS,HWC WASHER, BOLT NUT,APPLIANCE, FIXATION, NAIL/BLADE/PLATE COMBINATION, MULTIPLE COM WASHER, BOLT NUT,APPLIANCE, FIXATION, NAIL/BLADE/PLATE COMBINATION, MULTIPLE COMPONENT, METAL COMPOSITE,PIN, FIXATION, SMOOTH,ROD, FIXATION, INTRAMEDULLARY AND ACCESSORIES,APPLIANCE, FIXATION, NAIL/BLADE/PLATE COMBINATION, MULTIPLE COMPONENT,PIN, FIXATION, THREADED,PLATE, FIXATION, BONE,Screw, fixation, bone 2 SCREW, CANCELLOUS
23 00880304999541 32-700077 32-700077 OIY,MBH,MBV,JWH Prosthesis, knee, patellofemorotibial, semi-constrained, cemented, polymer + add Prosthesis, knee, patellofemorotibial, semi-constrained, cemented, polymer + additive/metal/polymer + additive,PROSTHESIS, KNEE, PATELLO/FEMOROTIBIAL, SEMI-CONSTRAINED, UNCEMENTED, POROUS, COATED, POLYMER/METAL/POLYMER,Prosthesis, knee, patello/femorotibial, semi-constrained, uhmwpe, pegged, cemented, polymer/metal/polymer,PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER 2 VANGUARD XP
24 00880304990135 SSI001696 SSI001696 KWS Prosthesis, Shoulder, Semi-Constrained, Metal/Polymer Cemented 2 Comprehensive Mini Baseplate
25 00880304989115 010000987 010000987 PBI,LZO,OQI,OQH,OQG,LPH,JDI,LWZ prosthesis, hip, constrained, cemented or uncemented, metal/polymer, + additive, prosthesis, hip, constrained, cemented or uncemented, metal/polymer, + additive,Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented,Hip, semi-constrained, cemented, metal/ceramic/polymer + additive, porous uncemented,Hip, semi-constrained, cemented, metal/polymer + additive, cemented,Hip Prosthesis, semi-constrained, cemented, metal/polymer, + additive, porous, uncemented,PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED,Prosthesis, hip, semi-constrained, metal/polymer, cemented,TISSUE GRAFT OF LESS THAN 6MM 2 G7® ACETABULAR LINER
26 00880304989108 010000986 010000986 OQI,PBI,JDI,LZO,OQG,LPH,OQH,LWZ Hip, semi-constrained, cemented, metal/ceramic/polymer + additive, porous unceme Hip, semi-constrained, cemented, metal/ceramic/polymer + additive, porous uncemented,prosthesis, hip, constrained, cemented or uncemented, metal/polymer, + additive,Prosthesis, hip, semi-constrained, metal/polymer, cemented,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, METAL/POLYMER, POROUS UNCEMENTED,Hip, semi-constrained, cemented, metal/polymer + additive, cemented,TISSUE GRAFT OF LESS THAN 6MM 2 G7® ACETABULAR LINER
27 00880304989092 010000985 010000985 OQI,LPH,LZO,JDI,OQH,OQG,PBI,LWZ Hip, semi-constrained, cemented, metal/ceramic/polymer + additive, porous unceme Hip, semi-constrained, cemented, metal/ceramic/polymer + additive, porous uncemented,PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED,Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented,Prosthesis, hip, semi-constrained, metal/polymer, cemented,Hip, semi-constrained, cemented, metal/polymer + additive, cemented,Hip Prosthesis, semi-constrained, cemented, metal/polymer, + additive, porous, uncemented,prosthesis, hip, constrained, cemented or uncemented, metal/polymer, + additive,TISSUE GRAFT OF LESS THAN 6MM 2 G7® ACETABULAR LINER
28 00880304989085 010000984 010000984 LPH,PBI,OQI,OQG,JDI,LZO,OQH,LWZ PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED,prosthesis, PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED,prosthesis, hip, constrained, cemented or uncemented, metal/polymer, + additive,Hip, semi-constrained, cemented, metal/ceramic/polymer + additive, porous uncemented,Hip Prosthesis, semi-constrained, cemented, metal/polymer, + additive, porous, uncemented,Prosthesis, hip, semi-constrained, metal/polymer, cemented,Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented,Hip, semi-constrained, cemented, metal/polymer + additive, cemented,TISSUE GRAFT OF LESS THAN 6MM 2 G7® ACETABULAR LINER
29 00880304989078 010000983 010000983 LPH,LZO,OQG,PBI,OQI,JDI,OQH,LWZ 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, constrained, cemented or uncemented, metal/polymer, + additive,Hip, semi-constrained, cemented, metal/ceramic/polymer + additive, porous uncemented,Prosthesis, hip, semi-constrained, metal/polymer, cemented,Hip, semi-constrained, cemented, metal/polymer + additive, cemented,TISSUE GRAFT OF LESS THAN 6MM 2 G7® ACETABULAR LINER
30 00880304989061 010000982 010000982 OQI,LZO,LPH,JDI,OQH,OQG,PBI,LWZ Hip, semi-constrained, cemented, metal/ceramic/polymer + additive, porous unceme Hip, semi-constrained, cemented, metal/ceramic/polymer + additive, porous uncemented,Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented,PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED,Prosthesis, hip, semi-constrained, metal/polymer, cemented,Hip, semi-constrained, cemented, metal/polymer + additive, cemented,Hip Prosthesis, semi-constrained, cemented, metal/polymer, + additive, porous, uncemented,prosthesis, hip, constrained, cemented or uncemented, metal/polymer, + additive,TISSUE GRAFT OF LESS THAN 6MM 2 G7® ACETABULAR LINER
31 00880304928282 110004037 110004037 HWC,HRS Screw, fixation, bone,Plate, fixation, bone 2 RECONSTRUCTIVE WEDGE
32 00880304926905 110003456 110003456 LWZ,OQI,PBI,LPH,JDI,OQH,OQG,LZO,KWZ TISSUE GRAFT OF LESS THAN 6MM,Hip, semi-constrained, cemented, metal/ceramic/pol TISSUE GRAFT OF LESS THAN 6MM,Hip, semi-constrained, cemented, metal/ceramic/polymer + additive, porous uncemented,prosthesis, hip, constrained, cemented or uncemented, metal/polymer, + additive,PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED,Prosthesis, hip, semi-constrained, metal/polymer, cemented,Hip, semi-constrained, cemented, metal/polymer + additive, cemented,Hip Prosthesis, semi-constrained, cemented, metal/polymer, + additive, porous, uncemented,Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented,Prosthesis, hip, constrained, cemented or uncemented, metal/polymer 2 G7 LATERAL POSITIONING GUIDE
33 00880304863422 909874 909874 MBI,JDR Fastener, fixation, nondegradable, soft tissue,Staple, fixation, bone 2 TOGGLELOC™ WITH ZIPLOOP™
34 00880304853041 42-411403 42-411403 MBH,OIY,JWH,OOG,HRY PROSTHESIS, KNEE, PATELLO/FEMOROTIBIAL, SEMI-CONSTRAINED, UNCEMENTED, POROUS, CO PROSTHESIS, KNEE, PATELLO/FEMOROTIBIAL, SEMI-CONSTRAINED, UNCEMENTED, POROUS, COATED, POLYMER/METAL/POLYMER,Prosthesis, knee, patellofemorotibial, semi-constrained, cemented, polymer + additive/metal/polymer + additive,PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER,Knee arthroplasty implantation system,PROSTHESIS, KNEE, FEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, METAL/POLYMER 2 OXFORD® PARTIAL KNEE SYSTEM
35 00880304853034 42-411402 42-411402 OOG,HRY,MBH,JWH,OIY Knee arthroplasty implantation system,PROSTHESIS, KNEE, FEMOROTIBIAL, SEMI-CONST Knee arthroplasty implantation system,PROSTHESIS, KNEE, FEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, METAL/POLYMER,PROSTHESIS, KNEE, PATELLO/FEMOROTIBIAL, SEMI-CONSTRAINED, UNCEMENTED, POROUS, COATED, POLYMER/METAL/POLYMER,PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER,Prosthesis, knee, patellofemorotibial, semi-constrained, cemented, polymer + additive/metal/polymer + additive 2 OXFORD® PARTIAL KNEE SYSTEM
36 00880304850354 211255 211255 KWS,KWT,JDC,MBF,PHX PROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER CEMENTED,PROSTHESIS, SHOUL PROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER CEMENTED,PROSTHESIS, SHOULDER, NON-CONSTRAINED, METAL/POLYMER CEMENTED,PROSTHESIS, ELBOW, CONSTRAINED, CEMENTED,PROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER, UNCEMENTED,shoulder prosthesis, reverse configuration 2 Comprehensive® SRS / Discovery®
37 00880304850347 211254 211254 KWT,KWS,JDC,MBF,PHX PROSTHESIS, SHOULDER, NON-CONSTRAINED, METAL/POLYMER CEMENTED,PROSTHESIS, SHOULD PROSTHESIS, SHOULDER, NON-CONSTRAINED, METAL/POLYMER CEMENTED,PROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER CEMENTED,PROSTHESIS, ELBOW, CONSTRAINED, CEMENTED,PROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER, UNCEMENTED,shoulder prosthesis, reverse configuration 2 Comprehensive® SRS / Discovery®
38 00880304850330 211253 211253 JDC,MBF,KWS,KWT,PHX PROSTHESIS, ELBOW, CONSTRAINED, CEMENTED,PROSTHESIS, SHOULDER, SEMI-CONSTRAINED, PROSTHESIS, ELBOW, CONSTRAINED, CEMENTED,PROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER, UNCEMENTED,PROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER CEMENTED,PROSTHESIS, SHOULDER, NON-CONSTRAINED, METAL/POLYMER CEMENTED,shoulder prosthesis, reverse configuration 2 Comprehensive® SRS / Discovery®
39 00880304850323 211252 211252 KWS,KWT,MBF,JDC,PHX PROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER CEMENTED,PROSTHESIS, SHOUL PROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER CEMENTED,PROSTHESIS, SHOULDER, NON-CONSTRAINED, METAL/POLYMER CEMENTED,PROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER, UNCEMENTED,PROSTHESIS, ELBOW, CONSTRAINED, CEMENTED,shoulder prosthesis, reverse configuration 2 Comprehensive® SRS / Discovery®
40 00880304850316 211251 211251 JDC,KWS,KWT,MBF,PHX PROSTHESIS, ELBOW, CONSTRAINED, CEMENTED,PROSTHESIS, SHOULDER, SEMI-CONSTRAINED, PROSTHESIS, ELBOW, CONSTRAINED, CEMENTED,PROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER CEMENTED,PROSTHESIS, SHOULDER, NON-CONSTRAINED, METAL/POLYMER CEMENTED,PROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER, UNCEMENTED,shoulder prosthesis, reverse configuration 2 Comprehensive® SRS / Discovery®
41 00880304850309 211250 211250 MBF,JDC,KWT,KWS,PHX PROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER, UNCEMENTED,PROSTHESIS, EL PROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER, UNCEMENTED,PROSTHESIS, ELBOW, CONSTRAINED, CEMENTED,PROSTHESIS, SHOULDER, NON-CONSTRAINED, METAL/POLYMER CEMENTED,PROSTHESIS, SHOULDER, SEMI-CONSTRAINED, METAL/POLYMER CEMENTED,shoulder prosthesis, reverse configuration 2 Comprehensive® SRS / Discovery®
42 00880304849273 SSI002770 SSI002770 LPH,JDI,KWL,KWY,KWZ,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/Polymer, Cemented,Prosthesis, Hip, Hemi-, Femoral, Metal,Prosthesis, Hip, Hemi-, Femoral, Metal/Polymer, Cemented Or Uncemented,Prosthesis, Hip, Constrained, Cemented Or Uncemented, Metal/Polymer,Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented Or Non-Porous, Uncemented,Prosthesis, Hip, Semi-Constrained, Uncemented, Metal/Polymer, Non-Porous, Calicum-Phosphate,Hip Prosthesis, Semi-Constrained, Cemented, Metal/Polymer, + Additive, Porous, Uncemented 2 Taperloc® Complete Hip System
43 00880304849266 SSI002769 SSI002769 OQG,MEH,LZO,KWZ,KWY,KWL,JDI,LPH Hip Prosthesis, Semi-Constrained, Cemented, Metal/Polymer, + Additive, Porous, U Hip Prosthesis, Semi-Constrained, Cemented, Metal/Polymer, + Additive, Porous, Uncemented,Prosthesis, Hip, Semi-Constrained, Uncemented, Metal/Polymer, Non-Porous, Calicum-Phosphate,Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented Or Non-Porous, Uncemented,Prosthesis, Hip, Constrained, Cemented Or Uncemented, Metal/Polymer,Prosthesis, Hip, Hemi-, Femoral, Metal/Polymer, Cemented Or Uncemented,Prosthesis, Hip, Hemi-, Femoral, Metal,Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Cemented,Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented 2 Taperloc® Complete Hip System
44 00880304849259 SSI002768 SSI002768 LPH,JDI,KWL,KWY,KWZ,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/Polymer, Cemented,Prosthesis, Hip, Hemi-, Femoral, Metal,Prosthesis, Hip, Hemi-, Femoral, Metal/Polymer, Cemented Or Uncemented,Prosthesis, Hip, Constrained, Cemented Or Uncemented, Metal/Polymer,Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented Or Non-Porous, Uncemented,Prosthesis, Hip, Semi-Constrained, Uncemented, Metal/Polymer, Non-Porous, Calicum-Phosphate,Hip Prosthesis, Semi-Constrained, Cemented, Metal/Polymer, + Additive, Porous, Uncemented 2 Taperloc® Complete Hip System
45 00880304849242 SSI002767 SSI002767 OQG,MEH,LZO,KWZ,KWY,KWL,JDI,LPH Hip Prosthesis, Semi-Constrained, Cemented, Metal/Polymer, + Additive, Porous, U Hip Prosthesis, Semi-Constrained, Cemented, Metal/Polymer, + Additive, Porous, Uncemented,Prosthesis, Hip, Semi-Constrained, Uncemented, Metal/Polymer, Non-Porous, Calicum-Phosphate,Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented Or Non-Porous, Uncemented,Prosthesis, Hip, Constrained, Cemented Or Uncemented, Metal/Polymer,Prosthesis, Hip, Hemi-, Femoral, Metal/Polymer, Cemented Or Uncemented,Prosthesis, Hip, Hemi-, Femoral, Metal,Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Cemented,Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented 2 Taperloc® Complete Hip System
46 00880304849235 SSI002766 SSI002766 LPH,JDI,KWL,KWY,KWZ,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/Polymer, Cemented,Prosthesis, Hip, Hemi-, Femoral, Metal,Prosthesis, Hip, Hemi-, Femoral, Metal/Polymer, Cemented Or Uncemented,Prosthesis, Hip, Constrained, Cemented Or Uncemented, Metal/Polymer,Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented Or Non-Porous, Uncemented,Prosthesis, Hip, Semi-Constrained, Uncemented, Metal/Polymer, Non-Porous, Calicum-Phosphate,Hip Prosthesis, Semi-Constrained, Cemented, Metal/Polymer, + Additive, Porous, Uncemented 2 Taperloc® Complete Hip System
47 00880304849228 SSI002765 SSI002765 OQG,MEH,LZO,KWZ,KWY,KWL,JDI,LPH Hip Prosthesis, Semi-Constrained, Cemented, Metal/Polymer, + Additive, Porous, U Hip Prosthesis, Semi-Constrained, Cemented, Metal/Polymer, + Additive, Porous, Uncemented,Prosthesis, Hip, Semi-Constrained, Uncemented, Metal/Polymer, Non-Porous, Calicum-Phosphate,Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented Or Non-Porous, Uncemented,Prosthesis, Hip, Constrained, Cemented Or Uncemented, Metal/Polymer,Prosthesis, Hip, Hemi-, Femoral, Metal/Polymer, Cemented Or Uncemented,Prosthesis, Hip, Hemi-, Femoral, Metal,Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Cemented,Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented 2 Taperloc® Complete Hip System
48 00880304849211 SSI003712 SSI003712 JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer 2 Maxim Accel Knee System
49 00880304849204 SSI003711 SSI003711 JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer 2 Maxim Accel Knee System
50 00880304849198 SSI003710 SSI003710 JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer 2 Maxim Accel Knee System
Other products with the same Product Code "MDM"
No Primary DI Version or Model Catalog Number Device Description Brand Name Organization Name
1 00814008029822 PD-1000T-110 Tower Dis-Engage Instrument. The FOCUS Pedicle Screw System is intended for use Tower Dis-Engage Instrument. The FOCUS Pedicle Screw System is intended for use in the non-cervical posterior spine (T1-S1) to provide immobilization and stabilization of spinal segments in skeletally mature patients as an adjunct to fusion in the treatment of the following acute and chronic instabilities or deformities: degenerative disc disease (defined as back pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies), spondylolisthesis, fracture, dislocation, deformities or curvatures (i.e., scoliosis, kyphosis, and/or lordosis), spinal stenosis, tumor, pseudarthrosis, and failed previous fusion. FOCUS NVISION BIOMEDICAL TECHNOLOGIES, INC.
2 00814008029815 PD-1000T-109 Small Ratcheting T-Handle. The FOCUS Pedicle Screw System is intended for use i Small Ratcheting T-Handle. The FOCUS Pedicle Screw System is intended for use in the non-cervical posterior spine (T1-S1) to provide immobilization and stabilization of spinal segments in skeletally mature patients as an adjunct to fusion in the treatment of the following acute and chronic instabilities or deformities: degenerative disc disease (defined as back pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies), spondylolisthesis, fracture, dislocation, deformities or curvatures (i.e., scoliosis, kyphosis, and/or lordosis), spinal stenosis, tumor, pseudarthrosis, and failed previous fusion. FOCUS NVISION BIOMEDICAL TECHNOLOGIES, INC.
3 00814008029778 PD-1000T-112 Awl Small. The FOCUS Pedicle Screw System is intended for use in the non-cervic Awl Small. The FOCUS Pedicle Screw System is intended for use in the non-cervical posterior spine (T1-S1) to provide immobilization and stabilization of spinal segments in skeletally mature patients as an adjunct to fusion in the treatment of the following acute and chronic instabilities or deformities: degenerative disc disease (defined as back pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies), spondylolisthesis, fracture, dislocation, deformities or curvatures (i.e., scoliosis, kyphosis, and/or lordosis), spinal stenosis, tumor, pseudarthrosis, and failed previous fusion. FOCUS NVISION BIOMEDICAL TECHNOLOGIES, INC.
4 00814008029754 PD-1000T-108 Cross Connector Screw Driver. The FOCUS Pedicle Screw System is intended for us Cross Connector Screw Driver. The FOCUS Pedicle Screw System is intended for use in the non-cervical posterior spine (T1-S1) to provide immobilization and stabilization of spinal segments in skeletally mature patients as an adjunct to fusion in the treatment of the following acute and chronic instabilities or deformities: degenerative disc disease (defined as back pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies), spondylolisthesis, fracture, dislocation, deformities or curvatures (i.e., scoliosis, kyphosis, and/or lordosis), spinal stenosis, tumor, pseudarthrosis, and failed previous fusion. FOCUS NVISION BIOMEDICAL TECHNOLOGIES, INC.
5 00814008029747 PD-1000T-107 Rod Template. The FOCUS Pedicle Screw System is intended for use in the non-cer Rod Template. The FOCUS Pedicle Screw System is intended for use in the non-cervical posterior spine (T1-S1) to provide immobilization and stabilization of spinal segments in skeletally mature patients as an adjunct to fusion in the treatment of the following acute and chronic instabilities or deformities: degenerative disc disease (defined as back pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies), spondylolisthesis, fracture, dislocation, deformities or curvatures (i.e., scoliosis, kyphosis, and/or lordosis), spinal stenosis, tumor, pseudarthrosis, and failed previous fusion. FOCUS NVISION BIOMEDICAL TECHNOLOGIES, INC.
6 00814008026289 PD-1000T-105 Linear Persuader Counter Torque. The FOCUS Pedicle Screw System is intended for Linear Persuader Counter Torque. The FOCUS Pedicle Screw System is intended for use in the non-cervical posterior spine (T1-S1) to provide immobilization and stabilization of spinal segments in skeletally mature patients as an adjunct to fusion in the treatment of the following acute and chronic instabilities or deformities: degenerative disc disease (defined as back pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies), spondylolisthesis, fracture, dislocation, deformities or curvatures (i.e., scoliosis, kyphosis, and/or lordosis), spinal stenosis, tumor, pseudarthrosis, and failed previous fusion. FOCUS NVISION BIOMEDICAL TECHNOLOGIES, INC.
7 00814008026265 PD-1000T-043 Drill, for 7.5MM. The FOCUS Pedicle Screw System is intended for use in the non Drill, for 7.5MM. The FOCUS Pedicle Screw System is intended for use in the non-cervical posterior spine (T1-S1) to provide immobilization and stabilization of spinal segments in skeletally mature patients as an adjunct to fusion in the treatment of the following acute and chronic instabilities or deformities: degenerative disc disease (defined as back pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies), spondylolisthesis, fracture, dislocation, deformities or curvatures (i.e., scoliosis, kyphosis, and/or lordosis), spinal stenosis, tumor, pseudarthrosis, and failed previous fusion. FOCUS NVISION BIOMEDICAL TECHNOLOGIES, INC.
8 00814008026258 PD-1000T-042 Drill, for 6.5MM. The FOCUS Pedicle Screw System is intended for use in the non Drill, for 6.5MM. The FOCUS Pedicle Screw System is intended for use in the non-cervical posterior spine (T1-S1) to provide immobilization and stabilization of spinal segments in skeletally mature patients as an adjunct to fusion in the treatment of the following acute and chronic instabilities or deformities: degenerative disc disease (defined as back pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies), spondylolisthesis, fracture, dislocation, deformities or curvatures (i.e., scoliosis, kyphosis, and/or lordosis), spinal stenosis, tumor, pseudarthrosis, and failed previous fusion. FOCUS NVISION BIOMEDICAL TECHNOLOGIES, INC.
9 00814008026227 PD-1000T-074 Open Head Turner. The FOCUS Pedicle Screw System is intended for use in the non Open Head Turner. The FOCUS Pedicle Screw System is intended for use in the non-cervical posterior spine (T1-S1) to provide immobilization and stabilization of spinal segments in skeletally mature patients as an adjunct to fusion in the treatment of the following acute and chronic instabilities or deformities: degenerative disc disease (defined as back pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies), spondylolisthesis, fracture, dislocation, deformities or curvatures (i.e., scoliosis, kyphosis, and/or lordosis), spinal stenosis, tumor, pseudarthrosis, and failed previous fusion. FOCUS NVISION BIOMEDICAL TECHNOLOGIES, INC.
10 00814008026210 PD-1000T-073 Open Rod De-Rotator. The FOCUS Pedicle Screw System is intended for use in the Open Rod De-Rotator. The FOCUS Pedicle Screw System is intended for use in the non-cervical posterior spine (T1-S1) to provide immobilization and stabilization of spinal segments in skeletally mature patients as an adjunct to fusion in the treatment of the following acute and chronic instabilities or deformities: degenerative disc disease (defined as back pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies), spondylolisthesis, fracture, dislocation, deformities or curvatures (i.e., scoliosis, kyphosis, and/or lordosis), spinal stenosis, tumor, pseudarthrosis, and failed previous fusion. FOCUS NVISION BIOMEDICAL TECHNOLOGIES, INC.
11 00814008026166 PD-1000T-068 Open Rod Holder. The FOCUS Pedicle Screw System is intended for use in the non- Open Rod Holder. The FOCUS Pedicle Screw System is intended for use in the non-cervical posterior spine (T1-S1) to provide immobilization and stabilization of spinal segments in skeletally mature patients as an adjunct to fusion in the treatment of the following acute and chronic instabilities or deformities: degenerative disc disease (defined as back pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies), spondylolisthesis, fracture, dislocation, deformities or curvatures (i.e., scoliosis, kyphosis, and/or lordosis), spinal stenosis, tumor, pseudarthrosis, and failed previous fusion. FOCUS NVISION BIOMEDICAL TECHNOLOGIES, INC.
12 00814008026159 PD-1000T-067 Open (Counter) Anti-Torque. The FOCUS Pedicle Screw System is intended for use Open (Counter) Anti-Torque. The FOCUS Pedicle Screw System is intended for use in the non-cervical posterior spine (T1-S1) to provide immobilization and stabilization of spinal segments in skeletally mature patients as an adjunct to fusion in the treatment of the following acute and chronic instabilities or deformities: degenerative disc disease (defined as back pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies), spondylolisthesis, fracture, dislocation, deformities or curvatures (i.e., scoliosis, kyphosis, and/or lordosis), spinal stenosis, tumor, pseudarthrosis, and failed previous fusion. FOCUS NVISION BIOMEDICAL TECHNOLOGIES, INC.
13 00814008026142 PD-1000T-066 Open Rod Rocker. The FOCUS Pedicle Screw System is intended for use in the non- Open Rod Rocker. The FOCUS Pedicle Screw System is intended for use in the non-cervical posterior spine (T1-S1) to provide immobilization and stabilization of spinal segments in skeletally mature patients as an adjunct to fusion in the treatment of the following acute and chronic instabilities or deformities: degenerative disc disease (defined as back pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies), spondylolisthesis, fracture, dislocation, deformities or curvatures (i.e., scoliosis, kyphosis, and/or lordosis), spinal stenosis, tumor, pseudarthrosis, and failed previous fusion. FOCUS NVISION BIOMEDICAL TECHNOLOGIES, INC.
14 00814008026135 PD-1000T-065 Open Rod Pusher. The FOCUS Pedicle Screw System is intended for use in the non- Open Rod Pusher. The FOCUS Pedicle Screw System is intended for use in the non-cervical posterior spine (T1-S1) to provide immobilization and stabilization of spinal segments in skeletally mature patients as an adjunct to fusion in the treatment of the following acute and chronic instabilities or deformities: degenerative disc disease (defined as back pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies), spondylolisthesis, fracture, dislocation, deformities or curvatures (i.e., scoliosis, kyphosis, and/or lordosis), spinal stenosis, tumor, pseudarthrosis, and failed previous fusion. FOCUS NVISION BIOMEDICAL TECHNOLOGIES, INC.
15 00814008026128 PD-1000T-064 Rod Cutter. The FOCUS Pedicle Screw System is intended for use in the non-cervi Rod Cutter. The FOCUS Pedicle Screw System is intended for use in the non-cervical posterior spine (T1-S1) to provide immobilization and stabilization of spinal segments in skeletally mature patients as an adjunct to fusion in the treatment of the following acute and chronic instabilities or deformities: degenerative disc disease (defined as back pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies), spondylolisthesis, fracture, dislocation, deformities or curvatures (i.e., scoliosis, kyphosis, and/or lordosis), spinal stenosis, tumor, pseudarthrosis, and failed previous fusion. FOCUS NVISION BIOMEDICAL TECHNOLOGIES, INC.
16 00814008026111 PD-1000T-063 Open French Rod Bender. The FOCUS Pedicle Screw System is intended for use in t Open French Rod Bender. The FOCUS Pedicle Screw System is intended for use in the non-cervical posterior spine (T1-S1) to provide immobilization and stabilization of spinal segments in skeletally mature patients as an adjunct to fusion in the treatment of the following acute and chronic instabilities or deformities: degenerative disc disease (defined as back pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies), spondylolisthesis, fracture, dislocation, deformities or curvatures (i.e., scoliosis, kyphosis, and/or lordosis), spinal stenosis, tumor, pseudarthrosis, and failed previous fusion. FOCUS NVISION BIOMEDICAL TECHNOLOGIES, INC.
17 00814008026104 PD-1000T-103 Open Persuader, Linear. The FOCUS Pedicle Screw System is intended for use in t Open Persuader, Linear. The FOCUS Pedicle Screw System is intended for use in the non-cervical posterior spine (T1-S1) to provide immobilization and stabilization of spinal segments in skeletally mature patients as an adjunct to fusion in the treatment of the following acute and chronic instabilities or deformities: degenerative disc disease (defined as back pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies), spondylolisthesis, fracture, dislocation, deformities or curvatures (i.e., scoliosis, kyphosis, and/or lordosis), spinal stenosis, tumor, pseudarthrosis, and failed previous fusion. FOCUS NVISION BIOMEDICAL TECHNOLOGIES, INC.
18 00814008026098 PD-1000T-062 Open Persuader, Offset. The FOCUS Pedicle Screw System is intended for use in t Open Persuader, Offset. The FOCUS Pedicle Screw System is intended for use in the non-cervical posterior spine (T1-S1) to provide immobilization and stabilization of spinal segments in skeletally mature patients as an adjunct to fusion in the treatment of the following acute and chronic instabilities or deformities: degenerative disc disease (defined as back pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies), spondylolisthesis, fracture, dislocation, deformities or curvatures (i.e., scoliosis, kyphosis, and/or lordosis), spinal stenosis, tumor, pseudarthrosis, and failed previous fusion. FOCUS NVISION BIOMEDICAL TECHNOLOGIES, INC.
19 00814008026081 PD-1000T-061 Set Screw Driver (Double End). The FOCUS Pedicle Screw System is intended for u Set Screw Driver (Double End). The FOCUS Pedicle Screw System is intended for use in the non-cervical posterior spine (T1-S1) to provide immobilization and stabilization of spinal segments in skeletally mature patients as an adjunct to fusion in the treatment of the following acute and chronic instabilities or deformities: degenerative disc disease (defined as back pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies), spondylolisthesis, fracture, dislocation, deformities or curvatures (i.e., scoliosis, kyphosis, and/or lordosis), spinal stenosis, tumor, pseudarthrosis, and failed previous fusion. FOCUS NVISION BIOMEDICAL TECHNOLOGIES, INC.
20 00814008026074 PD-1000T-060 Open Pedical Screw Driver. The FOCUS Pedicle Screw System is intended for use i Open Pedical Screw Driver. The FOCUS Pedicle Screw System is intended for use in the non-cervical posterior spine (T1-S1) to provide immobilization and stabilization of spinal segments in skeletally mature patients as an adjunct to fusion in the treatment of the following acute and chronic instabilities or deformities: degenerative disc disease (defined as back pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies), spondylolisthesis, fracture, dislocation, deformities or curvatures (i.e., scoliosis, kyphosis, and/or lordosis), spinal stenosis, tumor, pseudarthrosis, and failed previous fusion. FOCUS NVISION BIOMEDICAL TECHNOLOGIES, INC.
21 00814008026067 PD-1000T-059 Distractor, Titanium. The FOCUS Pedicle Screw System is intended for use in the Distractor, Titanium. The FOCUS Pedicle Screw System is intended for use in the non-cervical posterior spine (T1-S1) to provide immobilization and stabilization of spinal segments in skeletally mature patients as an adjunct to fusion in the treatment of the following acute and chronic instabilities or deformities: degenerative disc disease (defined as back pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies), spondylolisthesis, fracture, dislocation, deformities or curvatures (i.e., scoliosis, kyphosis, and/or lordosis), spinal stenosis, tumor, pseudarthrosis, and failed previous fusion. FOCUS NVISION BIOMEDICAL TECHNOLOGIES, INC.
22 00814008026050 PD-1000T-055 Compressor, Titanium. The FOCUS Pedicle Screw System is intended for use in the Compressor, Titanium. The FOCUS Pedicle Screw System is intended for use in the non-cervical posterior spine (T1-S1) to provide immobilization and stabilization of spinal segments in skeletally mature patients as an adjunct to fusion in the treatment of the following acute and chronic instabilities or deformities: degenerative disc disease (defined as back pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies), spondylolisthesis, fracture, dislocation, deformities or curvatures (i.e., scoliosis, kyphosis, and/or lordosis), spinal stenosis, tumor, pseudarthrosis, and failed previous fusion. FOCUS NVISION BIOMEDICAL TECHNOLOGIES, INC.
23 00814008026043 PD-1000T-102 Open Probe, Lenke, Small. The FOCUS Pedicle Screw System is intended for use in Open Probe, Lenke, Small. The FOCUS Pedicle Screw System is intended for use in the non-cervical posterior spine (T1-S1) to provide immobilization and stabilization of spinal segments in skeletally mature patients as an adjunct to fusion in the treatment of the following acute and chronic instabilities or deformities: degenerative disc disease (defined as back pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies), spondylolisthesis, fracture, dislocation, deformities or curvatures (i.e., scoliosis, kyphosis, and/or lordosis), spinal stenosis, tumor, pseudarthrosis, and failed previous fusion. FOCUS NVISION BIOMEDICAL TECHNOLOGIES, INC.
24 00814008026036 PD-1000T-101 Open Probe, Duckbill, Small. The FOCUS Pedicle Screw System is intended for use Open Probe, Duckbill, Small. The FOCUS Pedicle Screw System is intended for use in the non-cervical posterior spine (T1-S1) to provide immobilization and stabilization of spinal segments in skeletally mature patients as an adjunct to fusion in the treatment of the following acute and chronic instabilities or deformities: degenerative disc disease (defined as back pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies), spondylolisthesis, fracture, dislocation, deformities or curvatures (i.e., scoliosis, kyphosis, and/or lordosis), spinal stenosis, tumor, pseudarthrosis, and failed previous fusion. FOCUS NVISION BIOMEDICAL TECHNOLOGIES, INC.
25 00814008026029 PD-1000T-054 Open Probe, Lenke, Large. The FOCUS Pedicle Screw System is intended for use in Open Probe, Lenke, Large. The FOCUS Pedicle Screw System is intended for use in the non-cervical posterior spine (T1-S1) to provide immobilization and stabilization of spinal segments in skeletally mature patients as an adjunct to fusion in the treatment of the following acute and chronic instabilities or deformities: degenerative disc disease (defined as back pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies), spondylolisthesis, fracture, dislocation, deformities or curvatures (i.e., scoliosis, kyphosis, and/or lordosis), spinal stenosis, tumor, pseudarthrosis, and failed previous fusion. FOCUS NVISION BIOMEDICAL TECHNOLOGIES, INC.
26 00814008026012 PD-1000T-053 Open Probe, Duckbill, Large. The FOCUS Pedicle Screw System is intended for use Open Probe, Duckbill, Large. The FOCUS Pedicle Screw System is intended for use in the non-cervical posterior spine (T1-S1) to provide immobilization and stabilization of spinal segments in skeletally mature patients as an adjunct to fusion in the treatment of the following acute and chronic instabilities or deformities: degenerative disc disease (defined as back pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies), spondylolisthesis, fracture, dislocation, deformities or curvatures (i.e., scoliosis, kyphosis, and/or lordosis), spinal stenosis, tumor, pseudarthrosis, and failed previous fusion. FOCUS NVISION BIOMEDICAL TECHNOLOGIES, INC.
27 00814008026005 PD-1000T-100 Open Sounder, Straight Thick. The FOCUS Pedicle Screw System is intended for us Open Sounder, Straight Thick. The FOCUS Pedicle Screw System is intended for use in the non-cervical posterior spine (T1-S1) to provide immobilization and stabilization of spinal segments in skeletally mature patients as an adjunct to fusion in the treatment of the following acute and chronic instabilities or deformities: degenerative disc disease (defined as back pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies), spondylolisthesis, fracture, dislocation, deformities or curvatures (i.e., scoliosis, kyphosis, and/or lordosis), spinal stenosis, tumor, pseudarthrosis, and failed previous fusion. FOCUS NVISION BIOMEDICAL TECHNOLOGIES, INC.
28 00814008025992 PD-1000T-052 Open Sounder, Straight Slim. The FOCUS Pedicle Screw System is intended for use Open Sounder, Straight Slim. The FOCUS Pedicle Screw System is intended for use in the non-cervical posterior spine (T1-S1) to provide immobilization and stabilization of spinal segments in skeletally mature patients as an adjunct to fusion in the treatment of the following acute and chronic instabilities or deformities: degenerative disc disease (defined as back pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies), spondylolisthesis, fracture, dislocation, deformities or curvatures (i.e., scoliosis, kyphosis, and/or lordosis), spinal stenosis, tumor, pseudarthrosis, and failed previous fusion. FOCUS NVISION BIOMEDICAL TECHNOLOGIES, INC.
29 00814008025985 PD-1000T-044 Drill, for 8.5MM. The FOCUS Pedicle Screw System is intended for use in the non Drill, for 8.5MM. The FOCUS Pedicle Screw System is intended for use in the non-cervical posterior spine (T1-S1) to provide immobilization and stabilization of spinal segments in skeletally mature patients as an adjunct to fusion in the treatment of the following acute and chronic instabilities or deformities: degenerative disc disease (defined as back pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies), spondylolisthesis, fracture, dislocation, deformities or curvatures (i.e., scoliosis, kyphosis, and/or lordosis), spinal stenosis, tumor, pseudarthrosis, and failed previous fusion. FOCUS NVISION BIOMEDICAL TECHNOLOGIES, INC.
30 00814008025978 PD-1000T-041 Drill, for 5.5MM. The FOCUS Pedicle Screw System is intended for use in the non Drill, for 5.5MM. The FOCUS Pedicle Screw System is intended for use in the non-cervical posterior spine (T1-S1) to provide immobilization and stabilization of spinal segments in skeletally mature patients as an adjunct to fusion in the treatment of the following acute and chronic instabilities or deformities: degenerative disc disease (defined as back pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies), spondylolisthesis, fracture, dislocation, deformities or curvatures (i.e., scoliosis, kyphosis, and/or lordosis), spinal stenosis, tumor, pseudarthrosis, and failed previous fusion. FOCUS NVISION BIOMEDICAL TECHNOLOGIES, INC.
31 00814008025961 PD-1000T-040 Drill, for 4.75MM. The FOCUS Pedicle Screw System is intended for use in the no Drill, for 4.75MM. The FOCUS Pedicle Screw System is intended for use in the non-cervical posterior spine (T1-S1) to provide immobilization and stabilization of spinal segments in skeletally mature patients as an adjunct to fusion in the treatment of the following acute and chronic instabilities or deformities: degenerative disc disease (defined as back pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies), spondylolisthesis, fracture, dislocation, deformities or curvatures (i.e., scoliosis, kyphosis, and/or lordosis), spinal stenosis, tumor, pseudarthrosis, and failed previous fusion. FOCUS NVISION BIOMEDICAL TECHNOLOGIES, INC.
32 00814008025954 PD-1000T-027 Open Awl. The FOCUS Pedicle Screw System is intended for use in the non-cervica Open Awl. The FOCUS Pedicle Screw System is intended for use in the non-cervical posterior spine (T1-S1) to provide immobilization and stabilization of spinal segments in skeletally mature patients as an adjunct to fusion in the treatment of the following acute and chronic instabilities or deformities: degenerative disc disease (defined as back pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies), spondylolisthesis, fracture, dislocation, deformities or curvatures (i.e., scoliosis, kyphosis, and/or lordosis), spinal stenosis, tumor, pseudarthrosis, and failed previous fusion. FOCUS NVISION BIOMEDICAL TECHNOLOGIES, INC.
33 00814008025947 PD-1000T-024 Open Reduction Tab Breaker. The FOCUS Pedicle Screw System is intended for use Open Reduction Tab Breaker. The FOCUS Pedicle Screw System is intended for use in the non-cervical posterior spine (T1-S1) to provide immobilization and stabilization of spinal segments in skeletally mature patients as an adjunct to fusion in the treatment of the following acute and chronic instabilities or deformities: degenerative disc disease (defined as back pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies), spondylolisthesis, fracture, dislocation, deformities or curvatures (i.e., scoliosis, kyphosis, and/or lordosis), spinal stenosis, tumor, pseudarthrosis, and failed previous fusion. FOCUS NVISION BIOMEDICAL TECHNOLOGIES, INC.
34 00814008025930 PD-1000T-022 Final Tightener, Set Screw. The FOCUS Pedicle Screw System is intended for use Final Tightener, Set Screw. The FOCUS Pedicle Screw System is intended for use in the non-cervical posterior spine (T1-S1) to provide immobilization and stabilization of spinal segments in skeletally mature patients as an adjunct to fusion in the treatment of the following acute and chronic instabilities or deformities: degenerative disc disease (defined as back pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies), spondylolisthesis, fracture, dislocation, deformities or curvatures (i.e., scoliosis, kyphosis, and/or lordosis), spinal stenosis, tumor, pseudarthrosis, and failed previous fusion. FOCUS NVISION BIOMEDICAL TECHNOLOGIES, INC.
35 00814008025923 PD-1000T-099 Open 8.5MM TAP, Solid. The FOCUS Pedicle Screw System is intended for use in th Open 8.5MM TAP, Solid. The FOCUS Pedicle Screw System is intended for use in the non-cervical posterior spine (T1-S1) to provide immobilization and stabilization of spinal segments in skeletally mature patients as an adjunct to fusion in the treatment of the following acute and chronic instabilities or deformities: degenerative disc disease (defined as back pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies), spondylolisthesis, fracture, dislocation, deformities or curvatures (i.e., scoliosis, kyphosis, and/or lordosis), spinal stenosis, tumor, pseudarthrosis, and failed previous fusion. FOCUS NVISION BIOMEDICAL TECHNOLOGIES, INC.
36 00814008025916 PD-1000T-098 Open 7.5MM TAP, Solid. The FOCUS Pedicle Screw System is intended for use in th Open 7.5MM TAP, Solid. The FOCUS Pedicle Screw System is intended for use in the non-cervical posterior spine (T1-S1) to provide immobilization and stabilization of spinal segments in skeletally mature patients as an adjunct to fusion in the treatment of the following acute and chronic instabilities or deformities: degenerative disc disease (defined as back pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies), spondylolisthesis, fracture, dislocation, deformities or curvatures (i.e., scoliosis, kyphosis, and/or lordosis), spinal stenosis, tumor, pseudarthrosis, and failed previous fusion. FOCUS NVISION BIOMEDICAL TECHNOLOGIES, INC.
37 00814008025909 PD-1000T-097 Open 6.5MM TAP, Solid. The FOCUS Pedicle Screw System is intended for use in th Open 6.5MM TAP, Solid. The FOCUS Pedicle Screw System is intended for use in the non-cervical posterior spine (T1-S1) to provide immobilization and stabilization of spinal segments in skeletally mature patients as an adjunct to fusion in the treatment of the following acute and chronic instabilities or deformities: degenerative disc disease (defined as back pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies), spondylolisthesis, fracture, dislocation, deformities or curvatures (i.e., scoliosis, kyphosis, and/or lordosis), spinal stenosis, tumor, pseudarthrosis, and failed previous fusion. FOCUS NVISION BIOMEDICAL TECHNOLOGIES, INC.
38 00814008025893 PD-1000T-096 Open 5.5MM TAP, Solid. The FOCUS Pedicle Screw System is intended for use in th Open 5.5MM TAP, Solid. The FOCUS Pedicle Screw System is intended for use in the non-cervical posterior spine (T1-S1) to provide immobilization and stabilization of spinal segments in skeletally mature patients as an adjunct to fusion in the treatment of the following acute and chronic instabilities or deformities: degenerative disc disease (defined as back pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies), spondylolisthesis, fracture, dislocation, deformities or curvatures (i.e., scoliosis, kyphosis, and/or lordosis), spinal stenosis, tumor, pseudarthrosis, and failed previous fusion. FOCUS NVISION BIOMEDICAL TECHNOLOGIES, INC.
39 00814008025886 PD-1000T-095 Open 4.75MM TAP, Solid. The FOCUS Pedicle Screw System is intended for use in t Open 4.75MM TAP, Solid. The FOCUS Pedicle Screw System is intended for use in the non-cervical posterior spine (T1-S1) to provide immobilization and stabilization of spinal segments in skeletally mature patients as an adjunct to fusion in the treatment of the following acute and chronic instabilities or deformities: degenerative disc disease (defined as back pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies), spondylolisthesis, fracture, dislocation, deformities or curvatures (i.e., scoliosis, kyphosis, and/or lordosis), spinal stenosis, tumor, pseudarthrosis, and failed previous fusion. FOCUS NVISION BIOMEDICAL TECHNOLOGIES, INC.
40 00814008025879 PD-1000T-003 MIS Third Dilator. The FOCUS Pedicle Screw System is intended for use in the no MIS Third Dilator. The FOCUS Pedicle Screw System is intended for use in the non-cervical posterior spine (T1-S1) to provide immobilization and stabilization of spinal segments in skeletally mature patients as an adjunct to fusion in the treatment of the following acute and chronic instabilities or deformities: degenerative disc disease (defined as back pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies), spondylolisthesis, fracture, dislocation, deformities or curvatures (i.e., scoliosis, kyphosis, and/or lordosis), spinal stenosis, tumor, pseudarthrosis, and failed previous fusion. FOCUS NVISION BIOMEDICAL TECHNOLOGIES, INC.
41 00814008025862 PD-1000T-002 MIS Second Dilator. The FOCUS Pedicle Screw System is intended for use in the n MIS Second Dilator. The FOCUS Pedicle Screw System is intended for use in the non-cervical posterior spine (T1-S1) to provide immobilization and stabilization of spinal segments in skeletally mature patients as an adjunct to fusion in the treatment of the following acute and chronic instabilities or deformities: degenerative disc disease (defined as back pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies), spondylolisthesis, fracture, dislocation, deformities or curvatures (i.e., scoliosis, kyphosis, and/or lordosis), spinal stenosis, tumor, pseudarthrosis, and failed previous fusion. FOCUS NVISION BIOMEDICAL TECHNOLOGIES, INC.
42 00814008025855 PD-1000T-001 MIS Initial Dilator. The FOCUS Pedicle Screw System is intended for use in the MIS Initial Dilator. The FOCUS Pedicle Screw System is intended for use in the non-cervical posterior spine (T1-S1) to provide immobilization and stabilization of spinal segments in skeletally mature patients as an adjunct to fusion in the treatment of the following acute and chronic instabilities or deformities: degenerative disc disease (defined as back pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies), spondylolisthesis, fracture, dislocation, deformities or curvatures (i.e., scoliosis, kyphosis, and/or lordosis), spinal stenosis, tumor, pseudarthrosis, and failed previous fusion. FOCUS NVISION BIOMEDICAL TECHNOLOGIES, INC.
43 00814008025848 PD-1000T-004 MIS Final Dilator, Smooth. The FOCUS Pedicle Screw System is intended for use i MIS Final Dilator, Smooth. The FOCUS Pedicle Screw System is intended for use in the non-cervical posterior spine (T1-S1) to provide immobilization and stabilization of spinal segments in skeletally mature patients as an adjunct to fusion in the treatment of the following acute and chronic instabilities or deformities: degenerative disc disease (defined as back pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies), spondylolisthesis, fracture, dislocation, deformities or curvatures (i.e., scoliosis, kyphosis, and/or lordosis), spinal stenosis, tumor, pseudarthrosis, and failed previous fusion. FOCUS NVISION BIOMEDICAL TECHNOLOGIES, INC.
44 00814008025824 PD-1000T-018 MIS 8.5MM Tap, Cannulated. The FOCUS Pedicle Screw System is intended for use i MIS 8.5MM Tap, Cannulated. The FOCUS Pedicle Screw System is intended for use in the non-cervical posterior spine (T1-S1) to provide immobilization and stabilization of spinal segments in skeletally mature patients as an adjunct to fusion in the treatment of the following acute and chronic instabilities or deformities: degenerative disc disease (defined as back pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies), spondylolisthesis, fracture, dislocation, deformities or curvatures (i.e., scoliosis, kyphosis, and/or lordosis), spinal stenosis, tumor, pseudarthrosis, and failed previous fusion. FOCUS NVISION BIOMEDICAL TECHNOLOGIES, INC.
45 00814008025817 PD-1000T-017 MIS 7.5MM Tap, Cannulated. The FOCUS Pedicle Screw System is intended for use i MIS 7.5MM Tap, Cannulated. The FOCUS Pedicle Screw System is intended for use in the non-cervical posterior spine (T1-S1) to provide immobilization and stabilization of spinal segments in skeletally mature patients as an adjunct to fusion in the treatment of the following acute and chronic instabilities or deformities: degenerative disc disease (defined as back pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies), spondylolisthesis, fracture, dislocation, deformities or curvatures (i.e., scoliosis, kyphosis, and/or lordosis), spinal stenosis, tumor, pseudarthrosis, and failed previous fusion. FOCUS NVISION BIOMEDICAL TECHNOLOGIES, INC.
46 00814008025800 PD-1000T-016 MIS 6.5MM Tap, Cannulated. The FOCUS Pedicle Screw System is intended for use i MIS 6.5MM Tap, Cannulated. The FOCUS Pedicle Screw System is intended for use in the non-cervical posterior spine (T1-S1) to provide immobilization and stabilization of spinal segments in skeletally mature patients as an adjunct to fusion in the treatment of the following acute and chronic instabilities or deformities: degenerative disc disease (defined as back pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies), spondylolisthesis, fracture, dislocation, deformities or curvatures (i.e., scoliosis, kyphosis, and/or lordosis), spinal stenosis, tumor, pseudarthrosis, and failed previous fusion. FOCUS NVISION BIOMEDICAL TECHNOLOGIES, INC.
47 00814008025794 PD-1000T-015 MIS 5.5MM Tap, Cannulated. The FOCUS Pedicle Screw System is intended for use i MIS 5.5MM Tap, Cannulated. The FOCUS Pedicle Screw System is intended for use in the non-cervical posterior spine (T1-S1) to provide immobilization and stabilization of spinal segments in skeletally mature patients as an adjunct to fusion in the treatment of the following acute and chronic instabilities or deformities: degenerative disc disease (defined as back pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies), spondylolisthesis, fracture, dislocation, deformities or curvatures (i.e., scoliosis, kyphosis, and/or lordosis), spinal stenosis, tumor, pseudarthrosis, and failed previous fusion. FOCUS NVISION BIOMEDICAL TECHNOLOGIES, INC.
48 00814008025787 PD-1000T-014 MIS 4.75MM Tap, Cannulated. The FOCUS Pedicle Screw System is intended for use MIS 4.75MM Tap, Cannulated. The FOCUS Pedicle Screw System is intended for use in the non-cervical posterior spine (T1-S1) to provide immobilization and stabilization of spinal segments in skeletally mature patients as an adjunct to fusion in the treatment of the following acute and chronic instabilities or deformities: degenerative disc disease (defined as back pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies), spondylolisthesis, fracture, dislocation, deformities or curvatures (i.e., scoliosis, kyphosis, and/or lordosis), spinal stenosis, tumor, pseudarthrosis, and failed previous fusion. FOCUS NVISION BIOMEDICAL TECHNOLOGIES, INC.
49 00814008025770 PD-1000T-051 MIS Rod Length Calipers. The FOCUS Pedicle Screw System is intended for use in MIS Rod Length Calipers. The FOCUS Pedicle Screw System is intended for use in the non-cervical posterior spine (T1-S1) to provide immobilization and stabilization of spinal segments in skeletally mature patients as an adjunct to fusion in the treatment of the following acute and chronic instabilities or deformities: degenerative disc disease (defined as back pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies), spondylolisthesis, fracture, dislocation, deformities or curvatures (i.e., scoliosis, kyphosis, and/or lordosis), spinal stenosis, tumor, pseudarthrosis, and failed previous fusion. FOCUS NVISION BIOMEDICAL TECHNOLOGIES, INC.
50 00814008025763 PD-1000T-050 MIS Pedicle Screw Driver. The FOCUS Pedicle Screw System is intended for use in MIS Pedicle Screw Driver. The FOCUS Pedicle Screw System is intended for use in the non-cervical posterior spine (T1-S1) to provide immobilization and stabilization of spinal segments in skeletally mature patients as an adjunct to fusion in the treatment of the following acute and chronic instabilities or deformities: degenerative disc disease (defined as back pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies), spondylolisthesis, fracture, dislocation, deformities or curvatures (i.e., scoliosis, kyphosis, and/or lordosis), spinal stenosis, tumor, pseudarthrosis, and failed previous fusion. FOCUS NVISION BIOMEDICAL TECHNOLOGIES, INC.