Other products from "ORTHO DEVELOPMENT CORPORATION"
No Primary DI Version or Model Catalog Number Device Description Product Code Product Code Name Device Class Brand Name
1 00822409114702 C-1755-81 Uni Femoral Drill-Thru Trial Size 8 Left HSX PROSTHESIS, KNEE, FEMOROTIBIAL, NON-CONSTRAINED, CEMENTED, METAL/POLYMER 2 n/a
2 00822409114696 C-1755-71 Uni Femoral Drill-Thru Trial Size 7 Left HSX PROSTHESIS, KNEE, FEMOROTIBIAL, NON-CONSTRAINED, CEMENTED, METAL/POLYMER 2 n/a
3 00822409114689 C-1755-61 Uni Femoral Drill-Thru Trial Size 6 Left HSX PROSTHESIS, KNEE, FEMOROTIBIAL, NON-CONSTRAINED, CEMENTED, METAL/POLYMER 2 n/a
4 00822409114672 C-1755-51 Uni Femoral Drill-Thru Trial Size 5 Left HSX PROSTHESIS, KNEE, FEMOROTIBIAL, NON-CONSTRAINED, CEMENTED, METAL/POLYMER 2 n/a
5 00822409114665 C-1755-41 Uni Femoral Drill-Thru Trial Size 4 Left HSX PROSTHESIS, KNEE, FEMOROTIBIAL, NON-CONSTRAINED, CEMENTED, METAL/POLYMER 2 n/a
6 00822409114658 C-1755-31 Uni Femoral Drill-Thru Trial Size 3 Left HSX PROSTHESIS, KNEE, FEMOROTIBIAL, NON-CONSTRAINED, CEMENTED, METAL/POLYMER 2 n/a
7 00822409114641 C-1755-21 Uni Femoral Drill-Thru Trial Size 2 Left HSX PROSTHESIS, KNEE, FEMOROTIBIAL, NON-CONSTRAINED, CEMENTED, METAL/POLYMER 2 n/a
8 00822409114634 C-1755-11 Uni Femoral Drill-Thru Trial Size 1 Left HSX PROSTHESIS, KNEE, FEMOROTIBIAL, NON-CONSTRAINED, CEMENTED, METAL/POLYMER 2 n/a
9 00822409114795 C-1754 Uni Drill-Thru Femoral Trial Lug Drill HTW BIT, DRILL 1 n/a
10 00822409114368 C-1683 Posterior Referencing Sizer with Adjustable Boom LXH Orthopedic manual surgical instrument 1 n/a
11 00822409114351 C-1762-02 Uni Tibial Cut Guide 3 Degree Right Uncaptured LXH Orthopedic manual surgical instrument 1 n/a
12 00822409114344 C-1762-01 Uni Tibial Cut Guide 3 Degree Left Uncaptured LXH Orthopedic manual surgical instrument 1 n/a
13 00822409114771 C-1755-72 Uni Femoral Drill-Thru Trial Size 7 Right HSX PROSTHESIS, KNEE, FEMOROTIBIAL, NON-CONSTRAINED, CEMENTED, METAL/POLYMER 2 n/a
14 00822409114764 C-1755-62 Uni Femoral Drill-Thru Trial Size 6 Right HSX PROSTHESIS, KNEE, FEMOROTIBIAL, NON-CONSTRAINED, CEMENTED, METAL/POLYMER 2 n/a
15 00822409114726 C-1755-22 Uni Femoral Drill-Thru Trial Size 2 Right HSX PROSTHESIS, KNEE, FEMOROTIBIAL, NON-CONSTRAINED, CEMENTED, METAL/POLYMER 2 n/a
16 00822409114719 C-1755-12 Uni Femoral Drill-Thru Trial Size 1 Right HSX PROSTHESIS, KNEE, FEMOROTIBIAL, NON-CONSTRAINED, CEMENTED, METAL/POLYMER 2 n/a
17 00822409114733 C-1755-32 Uni Femoral Drill-Thru Trial Size 3 Right HSX PROSTHESIS, KNEE, FEMOROTIBIAL, NON-CONSTRAINED, CEMENTED, METAL/POLYMER 2 n/a
18 00822409114757 C-1755-52 Uni Femoral Drill-Thru Trial Size 5 Right HSX PROSTHESIS, KNEE, FEMOROTIBIAL, NON-CONSTRAINED, CEMENTED, METAL/POLYMER 2 n/a
19 00822409114740 C-1755-42 Uni Femoral Drill-Thru Trial Size 4 Right HSX PROSTHESIS, KNEE, FEMOROTIBIAL, NON-CONSTRAINED, CEMENTED, METAL/POLYMER 2 n/a
20 00822409114788 C-1755-82 Uni Femoral Drill-Thru Trial Size 8 Right HSX PROSTHESIS, KNEE, FEMOROTIBIAL, NON-CONSTRAINED, CEMENTED, METAL/POLYMER 2 n/a
21 00822409114337 C-1761-02 Uni Tibial Cut Guide 3° Right Captured LXH Orthopedic manual surgical instrument 1 n/a
22 00822409114320 C-1761-01 Uni Tibial Cut Guide 3° Left Captured LXH Orthopedic manual surgical instrument 1 n/a
23 00822409114245 C-1752-03 Uni Shim, 3 mm LXH Orthopedic manual surgical instrument 1 n/a
24 00822409114238 C-1752-02 Uni Shim, 2 mm LXH Orthopedic manual surgical instrument 1 n/a
25 00822409114207 C-1760 Uni Alignment Rod Adapter LXH Orthopedic manual surgical instrument 1 n/a
26 00822409114191 C-1759-15 Uni Spacer Block 15mm x 22mm LXH Orthopedic manual surgical instrument 1 n/a
27 00822409114184 C-1759-14 Uni Spacer Block 14mm x 21mm LXH Orthopedic manual surgical instrument 1 n/a
28 00822409114177 C-1759-13 Uni Spacer Block 13mm x 20mm LXH Orthopedic manual surgical instrument 1 n/a
29 00822409114160 C-1759-12 Uni Spacer Block 12mm x 19mm LXH Orthopedic manual surgical instrument 1 n/a
30 00822409114153 C-1759-11 Uni Spacer Block 11mm x 18mm LXH Orthopedic manual surgical instrument 1 n/a
31 00822409114146 C-1759-10 Uni Spacer Block 10mm x 17mm LXH Orthopedic manual surgical instrument 1 n/a
32 00822409114139 C-1759-09 Uni Spacer Block 9mm x 16mm LXH Orthopedic manual surgical instrument 1 n/a
33 00822409114122 C-1759-08 Uni Spacer Block 8mm x 15mm LXH Orthopedic manual surgical instrument 1 n/a
34 00822409114115 C-1756 Slim I/M Sleeve Adapter LXH Orthopedic Manual Surgical Instrument 1 n/a
35 00822409114108 C-1749-52 Uni Femoral Monoblock Distal Cut Guide R 13 x 5 LXH Orthopedic manual surgical instrument 1 n/a
36 00822409114092 C-1749-42 Uni Femoral Monoblock Distal Cut Guide R 12 x 5 LXH Orthopedic manual surgical instrument 1 n/a
37 00822409114085 C-1749-32 Uni Femoral Monoblock Distal Cut Guide R 11 x 6 LXH Orthopedic manual surgical instrument 1 n/a
38 00822409114078 C-1749-22 Uni Femoral Monoblock Distal Cut Guide R 10 x 7 LXH Orthopedic manual surgical instrument 1 n/a
39 00822409114061 C-1749-12 Uni Femoral Monoblock Distal Cut Guide R 9 x 8 LXH Orthopedic manual surgical instrument 1 n/a
40 00822409114054 C-1749-02 Uni Femoral Monoblock Distal Cut Guide R 9 x 7 LXH Orthopedic manual surgical instrument 1 n/a
41 00822409114047 C-1749-51 Uni Femoral Monoblock Distal Cut Guide L 13 x 5 LXH Orthopedic manual surgical instrument 1 n/a
42 00822409114030 C-1749-41 Uni Femoral Monoblock Distal Cut Guide L 12 x 5 LXH Orthopedic manual surgical instrument 1 n/a
43 00822409110940 C-1645 Ratcheting Handle LXH Orthopedic manual surgical instrument 1 n/a
44 00822409114023 C-1749-31 Uni Femoral Monoblock Distal Cut Guide L 11 x 6 LXH Orthopedic manual surgical instrument 1 n/a
45 00822409114016 C-1749-21 Uni Femoral Monoblock Distal Cut Guide L 10 x 7 LXH Orthopedic manual surgical instrument 1 n/a
46 00822409114009 C-1749-11 Uni Femoral Monoblock Distal Cut Guide L 9 x 8 LXH Orthopedic manual surgical instrument 1 n/a
47 00822409113996 C-1749-01 Uni Femoral Monoblock Distal Cut Guide L 9 x 7 LXH Orthopedic manual surgical instrument 1 n/a
48 00822409113989 C-1751 Uni Stabilizer Block Curved 9mm LXH Orthopedic manual surgical instrument 1 n/a
49 00822409113972 C-1750 Uni Stabilizer Block Flat 9mm LXH Orthopedic manual surgical instrument 1 n/a
50 00822409113965 C-1344-38 A/P Sizing Guide Left Paddle LXH Orthopedic manual surgical instrument 1 n/a
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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14 10885862618214 SPI-046319 SPI-046319 Truliant EXACTECH, INC.
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30 10885862606839 SPI-041550-1 SPI-041550-1 Truliant EXACTECH, INC.
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