Other products from "SMITH & NEPHEW, INC."
No Primary DI Version or Model Catalog Number Device Description Product Code Product Code Name Device Class Brand Name
1 00885556051375 71930717 71930717 SYNERGY PC FEM SZ18 130MM LPH PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED 2 SYNERGY
2 00885556799789 71075113B 71075113B SMART TSF FULL RING 130MM BLUE KTT APPLIANCE, FIXATION, NAIL/BLADE/PLATE COMBINATION, MULTIPLE COMPONENT 2 SMART TSF
3 00885556765357 E0016663-6 E0016663-6 HANDLE HRY PROSTHESIS, KNEE, FEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, METAL/POLYMER 2 Legion
4 00885556076538 913374 913374 STAPLE 1.16X3.8X3.4 JDR STAPLE, FIXATION, BONE 2 NA
5 00885556885208 E0017815-2 E0017815-2 SHORTENED 180 2/3 RING JDW PIN, FIXATION, THREADED 2 Ex-Fix
6 00885556883051 E0017793-1 E0017793-1 MODIFIED META NAIL DROP HSB ROD, FIXATION, INTRAMEDULLARY AND ACCESSORIES 2 Meta Nail
7 00885556867969 E0017558-7 E0017558-7 FLEXIBLE I/M ROD HRY PROSTHESIS, KNEE, FEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, METAL/POLYMER 2 Journey II
8 00885556816721 E0017448-3 E0017448-3 MODIFIED HEX DRIVER HWR DRIVER, PROSTHESIS 1 Polar
9 00885556810484 E0017443-1 E0017443-1 JII TIBIAL BLOCK - LEFT FZX Guide, surgical, instrument 1 JII
10 00885556806326 E0017367-11 E0017367-11 MODIFIED R3 INSERTER JDI Prosthesis, hip, semi-constrained, metal/polymer, cemented 2 R3
11 00885556805770 E0017337-1 E0017337-1 JII FLEXION SPACER BLOCK LXH ORTHOPEDIC MANUAL SURGICAL INSTRUMENT 1 JII
12 00885556804827 E0017314-9 E0017314-9 AP BLOCK SZ 8 FZX Guide, surgical, instrument 1 Legion
13 00885556802410 E0017267-1 E0017267-1 TIBIAL STEM TRIAL - 10MM X 70MM JWH PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER 2 Legion
14 00885556801673 E0017241-1 E0017241-1 MIS DA X-BAR JDG Prosthesis, hip, femoral component, cemented, metal 2 R3
15 00885556800812 E0017230-1 E0017230-1 2MM RECUT BLOCK HWT TEMPLATE 1 Journey II
16 00885556795255 E0017150-1 E0017150-1 11MM DEEP FLUTED END CUTTING REAMER HTO REAMER 1 Trigen
17 00885556793893 E0017119-7 E0017119-7 MIS ACETABULAR REAMER 58MM HTO REAMER 1 R3
18 00885556791905 E0017091-2 E0017091-2 TIBIAL CUTTING BLOCK - RT HRY PROSTHESIS, KNEE, FEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, METAL/POLYMER 2 Legion
19 00885556790229 E0017054-1 E0017054-1 MODULAR FIN PUNCH HANDLE HRY PROSTHESIS, KNEE, FEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, METAL/POLYMER 2 JII
20 00885556783313 E0016980-3 E0016980-3 UPPER TIBIAL GUIDE HRY PROSTHESIS, KNEE, FEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, METAL/POLYMER 2 Journey II
21 00885556777954 E0016892-1 E0016892-1 9MM REAMER HEAD HTO REAMER 1 Trigen
22 00885556775103 E0016853-3 E0016853-3 EXTENDED T8 DRIVER SHAFT HXX SCREWDRIVER 1 PERI-LOC
23 00885556773673 ROB20000 ROB20000 CORI ROBOTICS USA OLO Orthopedic stereotaxic instrument 2 Real Intelligence
24 00885556771013 E0016765-1 E0016765-1 MODIFIED ANGEL WING HRY PROSTHESIS, KNEE, FEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, METAL/POLYMER 2 Legion
25 00885556770566 E0016753-1 E0016753-1 FLUTED CURVED CANNULATED AWL HWJ AWL 1 Trigen
26 00885556763742 71170734 71170734 EVOS LARGE PROXIMAL HUMERUS PLATE TRAY FSM TRAY, SURGICAL, INSTRUMENT 1 EVOS
27 00885556763155 E0016528-7 E0016528-7 SZ 51MM BRIDGEBACK REAMER HTO REAMER 1 R3
28 00885556762189 72581004 72581004 EVOS 3.5MM/4.5MM UTILITY PLATE 4H 147MM HRS Plate, fixation, bone 2 EVOS
29 00885556757192 E0016586-2 E0016586-2 8.5MM REAMER HEAD HWE INSTRUMENT, SURGICAL, ORTHOPEDIC, AC-POWERED MOTOR AND ACCESSORY/ATTACHMENT 1 Trigen
30 00885556757116 E0016583-1 E0016583-1 RAT TAIL RASP JDG Prosthesis, hip, femoral component, cemented, metal 2 Polar
31 00885556755068 ROB10000 ROB10000 CORI Starter Kit OLO Orthopedic stereotaxic instrument 2 CORI
32 00885556753682 E0016536-2 E0016536-2 ZUK SPACER BLOCK - 11MM HWT TEMPLATE 1 Uni
33 00885556752081 72546585N 72546585N EVOS 6.5MM X 85MM CANNULATED SCREW HWC Screw, fixation, bone 2 EVOS
34 00885556740422 E0016327-2 E0016327-2 IM ROD SHORT HRY PROSTHESIS, KNEE, FEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, METAL/POLYMER 2 JII
35 00885556737392 E0016303-3 E0016303-3 OFFSET FIXATION ROD HRY PROSTHESIS, KNEE, FEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, METAL/POLYMER 2 JII
36 00885556733837 E0016253-2 E0016253-2 LARGE BLADE GAD RETRACTOR 1 Anthology
37 00885556725337 E0016116-2 E0016116-2 2MM RECUT BLOCK HWT TEMPLATE 1 Legion
38 00885556722701 21-8020 21-8020 DEPTH GAGE LXH ORTHOPEDIC MANUAL SURGICAL INSTRUMENT 1 N/A
39 00885556627020 PFSI00040 PFSI00040 Stride Poly Insert Size D 9mm HSX PROSTHESIS, KNEE, FEMOROTIBIAL, NON-CONSTRAINED, CEMENTED, METAL/POLYMER 2 STRIDE
40 00885556716274 E0015966-1 E0015966-1 FEMORAL STYLUS HRY PROSTHESIS, KNEE, FEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, METAL/POLYMER 2 Legion
41 00885556715536 E0015722-1 E0015722-1 FEMORAL TRIAL PADDLE HRY PROSTHESIS, KNEE, FEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, METAL/POLYMER 2 Legion
42 00885556626979 PFSI00033 PFSI00033 Stride Poly Insert Size C 8mm HSX PROSTHESIS, KNEE, FEMOROTIBIAL, NON-CONSTRAINED, CEMENTED, METAL/POLYMER 2 STRIDE
43 00885556713662 72411812 72411812 EVOS 1.8MM X 12MM LOCKING PEG T7 HRS Plate, fixation, bone 2 EVOS
44 00885556710357 E0015809-1 E0015809-1 SIDE FEMORAL HEAD IMPACTOR LXH ORTHOPEDIC MANUAL SURGICAL INSTRUMENT 1 R3
45 00885556710418 E0015860-1 E0015860-1 IM ALIGNMENT GUIDE WITH THUMB SCREWS HRY PROSTHESIS, KNEE, FEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, METAL/POLYMER 2 Legion
46 00885556710241 E0015781-3 E0015781-3 SPIKED ELEVATOR - STRAIGHT HTE ELEVATOR 1 Peri-loc
47 00885556708675 E0015708-5 E0015708-5 GII PS TRIAL INSERT 5-6 9MM JWH PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER 2 Legion
48 00885556706978 E0015771-1 E0015771-1 2MM RECUT BLOCK HWT TEMPLATE 1 Legion
49 00885556704561 E0015694-2 E0015694-2 PATELLA DEPTH GAUGE - 5MM HRY PROSTHESIS, KNEE, FEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, METAL/POLYMER 2 Legion
50 00885556704455 E0015672-1 E0015672-1 JOURNEY CR FEMORAL IMPACTOR JWH PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER 2 Journey II
Other products with the same Product Code "JWH"
No Primary DI Version or Model Catalog Number Device Description Brand Name Organization Name
1 28031497001900 SPK0722 Temporary Augmented Tibial Stem Spacer with gentamicin. Interspace Knee ATS is c Temporary Augmented Tibial Stem Spacer with gentamicin. Interspace Knee ATS is composed of fully formed gentamicin/polymethylmethacrylate (PMMA), radio-opaque bone cement. The device is sterile and single-use.InterSpace Knee ATS is indicated for temporary use (maximum 180 days) as an adjunct to total knee replacement (TKR) in skeletally mature patients undergoing a two-stage procedure due to a septic process, and where a large tibial defect is present.InterSpace Knee ATS is applied on the tibial plate following removal of the existing implant and radical debridement. The device must be combined with the tibial component of InterSpace Knee. The device is intended for use in conjunction with systemic antimicrobial antibiotic therapy (standard treatment approach to an infection).InterSpace Knee ATS is not intended for use for more than 180 days, at which time it must be explanted and a permanent device implanted or another appropriate treatment performed (e.g. resection arthroplasty, fusion etc.). Because of the inherent mechanical limitations of the device material (gentamicin/ polymethylmethacrylate), the Interspace Knee ATS is only indicated for patients who will consistently use traditional mobility assist devices (e.g. crutches, walkers, canes) throughout the implantation period. Interspace Knee ATS 80/12 TECRES SPA
2 28031497001894 SPK0622 Temporary Augmented Tibial Stem Spacer with gentamicin. Interspace Knee ATS is c Temporary Augmented Tibial Stem Spacer with gentamicin. Interspace Knee ATS is composed of fully formed gentamicin/polymethylmethacrylate (PMMA), radio-opaque bone cement. The device is sterile and single-use.InterSpace Knee ATS is indicated for temporary use (maximum 180 days) as an adjunct to total knee replacement (TKR) in skeletally mature patients undergoing a two-stage procedure due to a septic process, and where a large tibial defect is present.InterSpace Knee ATS is applied on the tibial plate following removal of the existing implant and radical debridement. The device must be combined with the tibial component of InterSpace Knee. The device is intended for use in conjunction with systemic antimicrobial antibiotic therapy (standard treatment approach to an infection).InterSpace Knee ATS is not intended for use for more than 180 days, at which time it must be explanted and a permanent device implanted or another appropriate treatment performed (e.g. resection arthroplasty, fusion etc.). Because of the inherent mechanical limitations of the device material (gentamicin/ polymethylmethacrylate), the Interspace Knee ATS is only indicated for patients who will consistently use traditional mobility assist devices (e.g. crutches, walkers, canes) throughout the implantation period. Interspace Knee ATS 80/07 TECRES SPA
3 28031497001887 SPK0522 Temporary Augmented Tibial Stem Spacer with gentamicin. Interspace Knee ATS is c Temporary Augmented Tibial Stem Spacer with gentamicin. Interspace Knee ATS is composed of fully formed gentamicin/polymethylmethacrylate (PMMA), radio-opaque bone cement.The device is sterile and single-use.InterSpace Knee ATS is indicated for temporary use (maximum 180 days) as an adjunct to total knee replacement (TKR) in skeletally mature patients undergoing a two-stage procedure due to a septic process, and where a large tibial defect is present.InterSpace Knee ATS is applied on the tibial plate following removal of the existing implant and radical debridement. The device must be combined with the tibial component of InterSpace Knee. The device is intended for use in conjunction with systemic antimicrobial antibiotic therapy (standard treatment approach to an infection).InterSpace Knee ATS is not intended for use for more than 180 days, at which time it must be explanted and a permanent device implanted or another appropriate treatment performed (e.g. resection arthroplasty, fusion etc.). Because of the inherent mechanical limitations of the device material (gentamicin/ polymethylmethacrylate), the Interspace Knee ATS is only indicated for patients who will consistently use traditional mobility assist devices (e.g. crutches, walkers, canes) throughout the implantation period. Interspace Knee ATS 60/12 TECRES SPA
4 28031497001870 SPK0422 Temporary Augmented Tibial Stem Spacer with gentamicin. Interspace Knee ATS is c Temporary Augmented Tibial Stem Spacer with gentamicin. Interspace Knee ATS is composed of fully formed gentamicin/polymethylmethacrylate (PMMA), radio-opaque bone cement. The device is sterile and single-use.InterSpace Knee ATS is indicated for temporary use (maximum 180 days) as an adjunct to total knee replacement (TKR) in skeletally mature patients undergoing a two-stage procedure due to a septic process, and where a large tibial defect is present.InterSpace Knee ATS is applied on the tibial plate following removal of the existing implant and radical debridement. The device must be combined with the tibial component of InterSpace Knee. The device is intended for use in conjunction with systemic antimicrobial antibiotic therapy (standard treatment approach to an infection).InterSpace Knee ATS is not intended for use for more than 180 days, at which time it must be explanted and a permanent device implanted or another appropriate treatment performed (e.g. resection arthroplasty, fusion etc.). Because of the inherent mechanical limitations of the device material (gentamicin/ polymethylmethacrylate), the Interspace Knee ATS is only indicated for patients who will consistently use traditional mobility assist devices (e.g. crutches, walkers, canes) throughout the implantation period. Interspace Knee ATS 60/07 TECRES SPA
5 28031497001160 SPK0322 Temporary knee spacer with gentamicin. InterSpace Knee is composed of fully form Temporary knee spacer with gentamicin. InterSpace Knee is composed of fully formed gentamicin/polymethylmethacrylate (PMMA) radiopaque bone cement.The device is sterile and single-use.InterSpace Knee is indicated for temporary use (maximum 180 days) as a total knee replacement (TKR) in skeletally mature patients undergoing a two-stage procedure due to a septic process.InterSpace Knee is applied on the femoral condyles and on the tibial plate following removal of the existing implant and radical debridement. The device is intended for use in conjunction with systemic antimicrobial antibiotic therapy (standard treatment approach to an infection).InterSpace Knee is not intended for use for more than 180 days, at which time it must be explanted and a permanent device implanted or another appropriate treatment performed (e.g. resection arthroplasty, fusion etc.). Because of the inherent mechanical limitations of the device material (gentamicin/polymethylmethacrylate), Interspace Knee is only indicated for patients who will consistently use traditional mobility assist devices (e.g. crutches, walkers, canes) throughout the implantation period. InterSpace Knee TECRES SPA
6 28031497000606 SPK0222 Temporary knee spacer with gentamicin. InterSpace Knee is composed of fully form Temporary knee spacer with gentamicin. InterSpace Knee is composed of fully formed gentamicin/polymethylmethacrylate (PMMA) radiopaque bone cement.The device is sterile and single-use.InterSpace Knee is indicated for temporary use (maximum of 180 days) as a total knee replacement (TKR) in skeletally mature patients undergoing a two-stage procedure due to a septic process. InterSpace Knee is applied on the femoral condyles and on the tibial plate following removal of the existing implantand radical debridement. The device is intended for use in conjunction with systemic antimicrobial antibiotic therapy (standard treatment approach to an infection). InterSpace Knee is not intended for use for more than 180 days, at which time it must be explanted and a permanent device implanted or another appropriate treatment performed (e.g., resection arthroplasty, fusion, etc.). InterSpace Knee TECRES SPA
7 28031497000590 SPK0122 Temporary knee spacer with gentamicin. InterSpace Knee is composed of fully form Temporary knee spacer with gentamicin. InterSpace Knee is composed of fully formed gentamicin/polymethylmethacrylate (PMMA) radiopaque bone cement.The device is sterile and single-use.InterSpace Knee is indicated for temporary use (maximum of 180 days) as a total knee replacement (TKR) in skeletally mature patients undergoing a two-stage procedure due to a septic process. InterSpace Knee is applied on the femoral condyles and on the tibial plate following removal of the existing implantand radical debridement. The device is intended for use in conjunction with systemic antimicrobial antibiotic therapy (standard treatment approach to an infection). InterSpace Knee is not intended for use for more than 180 days, at which time it must be explanted and a permanent device implanted or another appropriate treatment performed (e.g., resection arthroplasty, fusion, etc.). InterSpace Knee TECRES SPA
8 28031497000583 SPK0022 Temporary knee spacer with gentamicin. InterSpace Knee is composed of fully form Temporary knee spacer with gentamicin. InterSpace Knee is composed of fully formed gentamicin/polymethylmethacrylate (PMMA) radiopaque bone cement.The device is sterile and single-use.InterSpace Knee is indicated for temporary use (maximum of 180 days) as a total knee replacement (TKR) in skeletally mature patients undergoing a two-stage procedure due to a septic process. InterSpace Knee is applied on the femoral condyles and on the tibial plate following removal of the existing implantand radical debridement. The device is intended for use in conjunction with systemic antimicrobial antibiotic therapy (standard treatment approach to an infection). InterSpace Knee is not intended for use for more than 180 days, at which time it must be explanted and a permanent device implanted or another appropriate treatment performed (e.g., resection arthroplasty, fusion, etc.). InterSpace Knee TECRES SPA
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