Other products from "DEPUY ORTHOPAEDICS, INC."
No Primary DI Version or Model Catalog Number Device Description Product Code Product Code Name Device Class Brand Name
1 10603295059523 1570-03-080 157003080 SUMMIT FEMORAL STEM 12/14 TAPER CEMENTED SIZE 2 STD 97mm JDI,LZO Prosthesis, hip, semi-constrained, metal/polymer, cemented,Prosthesis, hip, semi Prosthesis, hip, semi-constrained, metal/polymer, cemented,Prosthesis, hip, semi-constrained, metal/ceramic/polymer, cemented or non-porous, uncemented 2 SUMMIT
2 10603295253693 9911-07-000 991107000 INFERIOR JAW DEEP GAD RETRACTOR 1 NA
3 10603295384793 420904 420904 TruMatch TIBIAL PIN GUIDE FOR USE WITH: LEFT JWH,OOG,NJL PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER,Knee arthroplasty implantation system,Prosthesis, knee, patellofemorotibial, semi-constrained, metal/polymer, mobile bearing 2 TRUMATCH
4 10603295422501 2500-00-794 250000794 Case 2 Complete FSM TRAY, SURGICAL, INSTRUMENT 1 NA
5 10603295249023 96-6575 966575 SPECIALIST 2 TC3 TIB INSERT STERIL TRAY INSERT FSM TRAY, SURGICAL, INSTRUMENT 1 SPECIALIST
6 10603295239062 96-1474A 961474A SIGMA STABILIZED INSERT TRIAL SOLID SIZE 6 17.5mm HWT TEMPLATE 1 SIGMA
7 10603295218067 86-8801 868801 SIGMA OVAL PAT DRILL W/HUDSON END HWE INSTRUMENT, SURGICAL, ORTHOPEDIC, AC-POWERED MOTOR AND ACCESSORY/ATTACHMENT 1 SIGMA
8 10603295228356 9505-02-134 950502134 SIGMA HIGH PERFORMANCE RP-F BALANCED AP BLOCK 1.5 HTZ INSTRUMENT, CUTTING, ORTHOPEDIC 1 SIGMA
9 10603295227762 9505-02-060 950502060 SIGMA HIGH PERFORMANCE FBT DRILL TOWER HWT TEMPLATE 1 SIGMA HIGH PERFORMANCE
10 10603295216230 86-1374 861374 P.F.C. MODULAR PLUS STEP TRIAL SZ 1.5 15mm HWT TEMPLATE 1 P.F.C.
11 10603295178408 6020-14-000 602014000 ACETABULAR EXTR CHISEL 13in HWB EXTRACTOR 1 NA
12 10603295175995 55-7099 557099 APICAL HOLE PLUG JDL Prosthesis, hip, semi-constrained (metal cemented acetabular component) 3 S-ROM
13 10603295174394 5460-30-000 546030000 CEMENT RESTRICTOR TRIAL SIZE 1 HWT TEMPLATE 1 NA
14 10603295174448 5460-40-000 546040000 CEMENT RESTRICTOR TRIAL SIZE 6 HWT TEMPLATE 1 NA
15 10603295170747 52-1553 521553 S-ROM CRUCIATE HEAD PERIPHERAL SCREW 5mm x 35mm LPH PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED 2 S-ROM
16 10603295151760 2722-90-971 272290971 ACCLAIM MALLET GFJ MALLET, SURGICAL, GENERAL & PLASTIC SURGERY 1 ACCLAIM
17 10603295149279 2611-40-000 261140000 EXCEL INSTRUMENT CASE COMPLETE FSM TRAY, SURGICAL, INSTRUMENT 1 EXCEL
18 10603295123415 2422-70-000 242270000 CEMENTLESS DEL SYS CASE FSM TRAY, SURGICAL, INSTRUMENT 1 NA
19 10603295110224 2287-51-075 228751075 LCS M1 FINISHING GUIDE SM HWT TEMPLATE 1 LCS
20 10603295110361 2287-71-000 228771000 PATELLA FACE PLATE LXH ORTHOPEDIC MANUAL SURGICAL INSTRUMENT 1 NA
21 10603295109549 2277-55-000 227755000 LCS FEMORAL TEMPLATE MED HWT TEMPLATE 1 LCS
22 10603295102175 2218-90-000 221890000 AB STRAIGHT INSERTER HWR DRIVER, PROSTHESIS 1 NA
23 10603295104872 2230-44-010 223044010 GLOBAL CAP HUMERAL HEAD TRIAL 44mm x 18mm HWT TEMPLATE 1 GLOBAL CAP
24 10603295091257 2130-52-520 213052520 GLOBAL AP HUMERAL HEAD TRIAL 52 x 21 HWT TEMPLATE 1 GLOBAL AP
25 10603295089728 2128-61-070 212861070 GLOBAL ADVANTAGE T-HANDLE HTO REAMER 1 GLOBAL ADVANTAGE
26 10603295032823 1363-50-000 136350000 MODULAR CATHCART FRACTURE HEAD HIP BALL 50mm OD LZY Prosthesis, hip, hemi-, femoral, metal ball 2 NA
27 10603295000495 1011-40-055 101140055 SELF TAPPING ROOF PILE SCREW 55mm JDJ Mesh, surgical, acetabular, hip, prosthesis 2 NA
28 10603295000488 1011-40-050 101140050 SELF TAPPING ROOF PILE SCREW 50mm JDJ Mesh, surgical, acetabular, hip, prosthesis 2 NA
29 10603295178378 6020-11-000 602011000 CURETTE 10mm x 17in HTF CURETTE 1 NA
30 10603295178361 6020-10-000 602010000 CURETTE 8mm x 17in HTF CURETTE 1 NA
31 10603295124610 2443-12-000 244312000 CANAL REAMER 8mm HTO REAMER 1 NA
32 10603295124603 2443-10-000 244310000 CANAL REAMER 7mm HTO REAMER 1 NA
33 10603295122760 2421-06-000 242106000 FLAT OSTEOTOME 20mm HWM OSTEOTOME 1 NA
34 10603295526353 2999-66-724 299966724 EMPHASYS MAKE TO ORDER ACETABULAR CUP INSERTER ADAPTOR HWA IMPACTOR 1 EMPHASYS
35 10603295514305 2999-65-183 299965183 MAKE TO ORDER TRI-LOCK BROACH REVERSE SZ 9 HTQ BROACH 1 NA
36 10603295514299 2999-65-182 299965182 MAKE TO ORDER TRI-LOCK BROACH REVERSE SZ 8 HTQ BROACH 1 NA
37 10603295514282 2999-65-181 299965181 MAKE TO ORDER TRI-LOCK BROACH REVERSE SZ 7 HTQ BROACH 1 NA
38 10603295514275 2999-65-178 299965178 MAKE TO ORDER TRI-LOCK BROACH REVERSE SZ 4 HTQ BROACH 1 NA
39 10603295514268 2999-65-177 299965177 MAKE TO ORDER TRI-LOCK BROACH REVERSE SZ 3 HTQ BROACH 1 NA
40 10603295514251 2999-65-176 299965176 MAKE TO ORDER TRI-LOCK BROACH REVERSE SZ 2 HTQ BROACH 1 NA
41 10603295514244 2999-65-186 299965186 MAKE TO ORDER TRI-LOCK BROACH REVERSE SZ 12 HTQ BROACH 1 NA
42 10603295514237 2999-65-185 299965185 MAKE TO ORDER TRI-LOCK BROACH REVERSE SZ 11 HTQ BROACH 1 NA
43 10603295514220 2999-65-184 299965184 MAKE TO ORDER TRI-LOCK BROACH REVERSE SZ 10 HTQ BROACH 1 NA
44 10603295514213 2999-65-175 299965175 MAKE TO ORDER TRI-LOCK BROACH REVERSE SZ 1 HTQ BROACH 1 NA
45 10603295514206 2999-65-174 299965174 MAKE TO ORDER TRI-LOCK BROACH REVERSE SZ 0 HTQ BROACH 1 NA
46 10603295514190 2999-65-180 299965180 MAKE TO ORDER TRI-LOCK BROACH REVERSE SZ 6 HTQ BROACH 1 NA
47 10603295514183 2999-65-173 299965173 MAKE TO ORDER TRI-LOCK BROACH REVERSE START HTQ BROACH 1 NA
48 10603295514176 2999-65-179 299965179 MAKE TO ORDER TRI-LOCK BROACH REVERSE SZ 5 HTQ BROACH 1 NA
49 10603295248651 96-6521 966521 M.B.T. REVISION TIBIAL BROACH HANDLE HTQ BROACH 1 NA
50 10603295506188 2999-66-451 299966451 Tissue Sparing Solutions MAKE TO ORDER DUAL OFFSET BROACH HANDLE ADAPTER FOR SLAP HAMMER HTQ BROACH 1 NA
Other products with the same Product Codes "NJL, JWH, OOG"
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
9 10885862621931 SPI-046699 SPI-046699 Special Pinned Femoral RT- INT/ LT-EXT Rotation Adjustment Block Truliant EXACTECH, INC.
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11 10885862621528 SPI-046441 SPI-046441 SPECIAL VAN DE LEUR TIBIAL RESECTOR, UPPER ASSEMBLY Truliant EXACTECH, INC.
12 10885862618719 SPI-046412 SPI-046412 SPECIAL LPI TIBIAL RESECETION BLOCK, RIGHT, WIDE SLOT Truliant EXACTECH, INC.
13 10885862618702 SPI-046411 SPI-046411 SPECIAL LPI TIBIAL RESECETION BLOCK, LEFT, WIDE SLOT Truliant EXACTECH, INC.
14 10885862618214 SPI-046319 SPI-046319 Truliant EXACTECH, INC.
15 10885862618207 SPI-046022 SPI-046022 SPECIAL VAN DE LEUR TIBIAL RESECTOR, SHAFT ASSEMBLY Truliant EXACTECH, INC.
16 10885862618146 SPI-046017 SPI-046017 SPECIAL VAN DE LEUR TIBIAL RESECTOR, ANKLE YOKE Truliant EXACTECH, INC.
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