No | Primary DI | Version or Model | Catalog Number | Device Description | Product Code | Product Code Name | Device Class | Brand Name |
---|---|---|---|---|---|---|---|---|
1 | 03701089525398 | 1-01-07-2084 | JWH | Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer | 2 | Crescendo Meniscal Insert PS 17mm Size 4 | ||
2 | 03701089525275 | 1-01-07-2066 | JWH | Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer | 2 | Crescendo Meniscal Insert PS 13mm Size 6 | ||
3 | 03701089525213 | 1-01-07-2060 | JWH | Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer | 2 | Crescendo Meniscal Insert PS 13mm Size 0 | ||
4 | 03701089525145 | 1-01-07-2010 | JWH | Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer | 2 | Crescendo Meniscal Insert PS 12mm Size 0 | ||
5 | 03701089524988 | 1-01-07-2285 | JWH | Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer | 2 | Crescendo Meniscal Insert CR Ultracongruent 17mm Size 5 | ||
6 | 03701089524919 | 1-01-07-2275 | JWH | Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer | 2 | Crescendo Meniscal Insert CR Ultracongruent 15mm Size 5 | ||
7 | 03701089524902 | 1-01-07-2274 | JWH | Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer | 2 | Crescendo Meniscal Insert CR Ultracongruent 15mm Size 4 | ||
8 | 03701089524681 | 1-01-07-2253 | JWH | Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer | 2 | Crescendo Meniscal Insert CR Ultracongruent 11mm Size 3 | ||
9 | 03701089524636 | 1-01-07-2205 | JWH | Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer | 2 | Crescendo Meniscal Insert CR Ultracongruent 10mm Size 5 | ||
10 | 03701089524582 | 1-01-07-2200 | JWH | Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer | 2 | Crescendo Meniscal Insert CR Ultracongruent 10mm Size 0 | ||
11 | 03701089524544 | 1-01-07-2183 | JWH | Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer | 2 | Crescendo Meniscal Insert CR Standard 17mm Size 3 | ||
12 | 03701089524513 | 1-01-07-2180 | JWH | Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer | 2 | Crescendo Meniscal Insert CR Standard 17mm Size 0 | ||
13 | 03701089524452 | 1-01-07-2171 | JWH | Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer | 2 | Crescendo Meniscal Insert CR Standard 15mm Size 1 | ||
14 | 03701089524438 | 1-01-07-2166 | JWH | Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer | 2 | Crescendo Meniscal Insert CR Standard 13mm Size 6 | ||
15 | 03701089524360 | 1-01-07-2116 | JWH | Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer | 2 | Crescendo Meniscal Insert CR Standard 12mm Size 6 | ||
16 | 03701089524322 | 1-01-07-2112 | JWH | Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer | 2 | Crescendo Meniscal Insert CR Standard 12mm Size 2 | ||
17 | 03701089524025 | 1-01-07-1064 | JWH | Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer | 2 | Crescendo Femoral Component Cemented - PS Size 4R | ||
18 | 03701089523950 | 1-01-07-3004 | JWH | Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer | 2 | Crescendo Femoral Component Cemented - CR Size 4L | ||
19 | 03701089523820 | 1-01-07-4005 | JWH | Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer | 2 | Crescendo Tibial Component Cemented - Size 5 | ||
20 | 03701089523813 | 1-01-07-4004 | JWH | Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer | 2 | Crescendo Tibial Component Cemented - Size 4 | ||
21 | 03701089523783 | 1-01-07-4001 | JWH | Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer | 2 | Crescendo Tibial Component Cemented - Size 1 | ||
22 | 03701089520867 | 1-01-152-644 | LPH,MEH | Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented,Prosthesis, Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented,Prosthesis, Hip, Semi-Constrained, Uncemented, Metal/Polymer, Non-Porous, Calicum-Phosphate | 2 | SIGNATURE Head - BIOLOX Delta | ||
23 | 03701089520850 | 1-01-152-643 | MEH,LPH | Prosthesis, Hip, Semi-Constrained, Uncemented, Metal/Polymer, Non-Porous, Calicu Prosthesis, Hip, Semi-Constrained, Uncemented, Metal/Polymer, Non-Porous, Calicum-Phosphate,Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented | 2 | SIGNATURE Head - BIOLOX Delta | ||
24 | 03701089520843 | 1-01-152-642 | LPH,MEH | Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented,Prosthesis, Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented,Prosthesis, Hip, Semi-Constrained, Uncemented, Metal/Polymer, Non-Porous, Calicum-Phosphate | 2 | SIGNATURE Head - BIOLOX Delta | ||
25 | 03701089520836 | 1-01-152-641 | MEH,LPH | Prosthesis, Hip, Semi-Constrained, Uncemented, Metal/Polymer, Non-Porous, Calicu Prosthesis, Hip, Semi-Constrained, Uncemented, Metal/Polymer, Non-Porous, Calicum-Phosphate,Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented | 2 | SIGNATURE Head - BIOLOX Delta | ||
26 | 03701089520829 | 1-01-152-634 | LPH,MEH | Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented,Prosthesis, Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented,Prosthesis, Hip, Semi-Constrained, Uncemented, Metal/Polymer, Non-Porous, Calicum-Phosphate | 2 | SIGNATURE Head - BIOLOX Delta | ||
27 | 03701089520812 | 1-01-152-633 | MEH,LPH | Prosthesis, Hip, Semi-Constrained, Uncemented, Metal/Polymer, Non-Porous, Calicu Prosthesis, Hip, Semi-Constrained, Uncemented, Metal/Polymer, Non-Porous, Calicum-Phosphate,Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented | 2 | SIGNATURE Head - BIOLOX Delta | ||
28 | 03701089520805 | 1-01-152-632 | LPH,MEH | Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented,Prosthesis, Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented,Prosthesis, Hip, Semi-Constrained, Uncemented, Metal/Polymer, Non-Porous, Calicum-Phosphate | 2 | SIGNATURE Head - BIOLOX Delta | ||
29 | 03701089520799 | 1-01-152-631 | MEH,LPH | Prosthesis, Hip, Semi-Constrained, Uncemented, Metal/Polymer, Non-Porous, Calicu Prosthesis, Hip, Semi-Constrained, Uncemented, Metal/Polymer, Non-Porous, Calicum-Phosphate,Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented | 2 | SIGNATURE Head - BIOLOX Delta | ||
30 | 03701089520782 | 1-01-152-624 | LPH,MEH | Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented,Prosthesis, Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented,Prosthesis, Hip, Semi-Constrained, Uncemented, Metal/Polymer, Non-Porous, Calicum-Phosphate | 2 | SIGNATURE Head - BIOLOX Delta | ||
31 | 03701089520775 | 1-01-152-623 | MEH,LPH | Prosthesis, Hip, Semi-Constrained, Uncemented, Metal/Polymer, Non-Porous, Calicu Prosthesis, Hip, Semi-Constrained, Uncemented, Metal/Polymer, Non-Porous, Calicum-Phosphate,Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented | 2 | SIGNATURE Head - BIOLOX Delta | ||
32 | 03701089520768 | 1-01-152-622 | LPH,MEH | Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented,Prosthesis, Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented,Prosthesis, Hip, Semi-Constrained, Uncemented, Metal/Polymer, Non-Porous, Calicum-Phosphate | 2 | SIGNATURE Head - BIOLOX Delta | ||
33 | 03701089520751 | 1-01-152-621 | MEH,LPH | Prosthesis, Hip, Semi-Constrained, Uncemented, Metal/Polymer, Non-Porous, Calicu Prosthesis, Hip, Semi-Constrained, Uncemented, Metal/Polymer, Non-Porous, Calicum-Phosphate,Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented | 2 | SIGNATURE Head - BIOLOX Delta | ||
34 | 03701089520744 | 1-01-152-613 | LPH,MEH | Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented,Prosthesis, Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented,Prosthesis, Hip, Semi-Constrained, Uncemented, Metal/Polymer, Non-Porous, Calicum-Phosphate | 2 | SIGNATURE Head - BIOLOX Delta | ||
35 | 03701089520737 | 1-01-152-612 | MEH,LPH | Prosthesis, Hip, Semi-Constrained, Uncemented, Metal/Polymer, Non-Porous, Calicu Prosthesis, Hip, Semi-Constrained, Uncemented, Metal/Polymer, Non-Porous, Calicum-Phosphate,Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented | 2 | SIGNATURE Head - BIOLOX Delta | ||
36 | 03701089520720 | 1-01-152-611 | LPH,MEH | Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented,Prosthesis, Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented,Prosthesis, Hip, Semi-Constrained, Uncemented, Metal/Polymer, Non-Porous, Calicum-Phosphate | 2 | SIGNATURE Head - BIOLOX Delta | ||
37 | 03701089520713 | 1-01-152-044 | MEH,LPH | Prosthesis, Hip, Semi-Constrained, Uncemented, Metal/Polymer, Non-Porous, Calicu Prosthesis, Hip, Semi-Constrained, Uncemented, Metal/Polymer, Non-Porous, Calicum-Phosphate,Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented | 2 | SIGNATURE Head - CoCr | ||
38 | 03701089520706 | 1-01-152-043 | LPH,MEH | Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented,Prosthesis, Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented,Prosthesis, Hip, Semi-Constrained, Uncemented, Metal/Polymer, Non-Porous, Calicum-Phosphate | 2 | SIGNATURE Head - CoCr | ||
39 | 03701089520690 | 1-01-152-042 | MEH,LPH | Prosthesis, Hip, Semi-Constrained, Uncemented, Metal/Polymer, Non-Porous, Calicu Prosthesis, Hip, Semi-Constrained, Uncemented, Metal/Polymer, Non-Porous, Calicum-Phosphate,Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented | 2 | SIGNATURE Head - CoCr | ||
40 | 03701089520683 | 1-01-152-041 | LPH,MEH | Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented,Prosthesis, Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented,Prosthesis, Hip, Semi-Constrained, Uncemented, Metal/Polymer, Non-Porous, Calicum-Phosphate | 2 | SIGNATURE Head - CoCr | ||
41 | 03701089520676 | 1-01-152-034 | MEH,LPH | Prosthesis, Hip, Semi-Constrained, Uncemented, Metal/Polymer, Non-Porous, Calicu Prosthesis, Hip, Semi-Constrained, Uncemented, Metal/Polymer, Non-Porous, Calicum-Phosphate,Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented | 2 | SIGNATURE Head - CoCr | ||
42 | 03701089520669 | 1-01-152-033 | LPH,MEH | Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented,Prosthesis, Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented,Prosthesis, Hip, Semi-Constrained, Uncemented, Metal/Polymer, Non-Porous, Calicum-Phosphate | 2 | SIGNATURE Head - CoCr | ||
43 | 03701089520652 | 1-01-152-032 | MEH,LPH | Prosthesis, Hip, Semi-Constrained, Uncemented, Metal/Polymer, Non-Porous, Calicu Prosthesis, Hip, Semi-Constrained, Uncemented, Metal/Polymer, Non-Porous, Calicum-Phosphate,Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented | 2 | SIGNATURE Head - CoCr | ||
44 | 03701089520645 | 1-01-152-031 | LPH,MEH | Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented,Prosthesis, Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented,Prosthesis, Hip, Semi-Constrained, Uncemented, Metal/Polymer, Non-Porous, Calicum-Phosphate | 2 | SIGNATURE Head - CoCr | ||
45 | 03701089520638 | 1-01-152-024 | MEH,LPH | Prosthesis, Hip, Semi-Constrained, Uncemented, Metal/Polymer, Non-Porous, Calicu Prosthesis, Hip, Semi-Constrained, Uncemented, Metal/Polymer, Non-Porous, Calicum-Phosphate,Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented | 2 | SIGNATURE Head - CoCr | ||
46 | 03701089520621 | 1-01-152-023 | LPH,MEH | Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented,Prosthesis, Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented,Prosthesis, Hip, Semi-Constrained, Uncemented, Metal/Polymer, Non-Porous, Calicum-Phosphate | 2 | SIGNATURE Head - CoCr | ||
47 | 03701089520614 | 1-01-152-022 | MEH,LPH | Prosthesis, Hip, Semi-Constrained, Uncemented, Metal/Polymer, Non-Porous, Calicu Prosthesis, Hip, Semi-Constrained, Uncemented, Metal/Polymer, Non-Porous, Calicum-Phosphate,Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented | 2 | SIGNATURE Head - CoCr | ||
48 | 03701089520607 | 1-01-152-021 | LPH,MEH | Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented,Prosthesis, Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented,Prosthesis, Hip, Semi-Constrained, Uncemented, Metal/Polymer, Non-Porous, Calicum-Phosphate | 2 | SIGNATURE Head - CoCr | ||
49 | 03701089520591 | 1-01-151-013 | MEH,LPH | Prosthesis, Hip, Semi-Constrained, Uncemented, Metal/Polymer, Non-Porous, Calicu Prosthesis, Hip, Semi-Constrained, Uncemented, Metal/Polymer, Non-Porous, Calicum-Phosphate,Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented | 2 | SIGNATURE Head - CoCr | ||
50 | 03701089520584 | 1-01-151-012 | LPH,MEH | Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented,Prosthesis, Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented,Prosthesis, Hip, Semi-Constrained, Uncemented, Metal/Polymer, Non-Porous, Calicum-Phosphate | 2 | SIGNATURE Head - CoCr |
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. |
10 | 10885862621924 | SPI-046300 | SPI-046300 | Special Pinned Femoral LT-INT / RT- EXT Rotation Adjustment Block | Truliant | EXACTECH, INC. |
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. |
17 | 10885862617989 | SPI-038032-60 | SPI-038032-60 | Truliant | EXACTECH, INC. | |
18 | 10885862617972 | SPI-045747-35 | SPI-045747-35 | Truliant | EXACTECH, INC. | |
19 | 10885862617965 | SPI-045745-29 | SPI-045745-29 | Truliant | EXACTECH, INC. | |
20 | 10885862617668 | SPI-045404 | SPI-045404 | Truliant | EXACTECH, INC. | |
21 | 10885862617453 | SPI-044689 | SPI-044689 | Truliant | EXACTECH, INC. | |
22 | 10885862617217 | SPI-044794 | SPI-044794 | Truliant | EXACTECH, INC. | |
23 | 10885862617132 | SPI-044447 | SPI-044447 | Truliant | EXACTECH, INC. | |
24 | 10885862610195 | SPI-044406 | SPI-044406 | Truliant | EXACTECH, INC. | |
25 | 10885862606884 | SPI-041553-32 | SPI-041553-32 | Truliant | EXACTECH, INC. | |
26 | 10885862606877 | SPI-041550-5 | SPI-041550-5 | Truliant | EXACTECH, INC. | |
27 | 10885862606860 | SPI-041550-4 | SPI-041550-4 | Truliant | EXACTECH, INC. | |
28 | 10885862606853 | SPI-041550-3 | SPI-041550-3 | Truliant | EXACTECH, INC. | |
29 | 10885862606846 | SPI-041550-2 | SPI-041550-2 | Truliant | EXACTECH, INC. | |
30 | 10885862606839 | SPI-041550-1 | SPI-041550-1 | Truliant | EXACTECH, INC. | |
31 | 10885862605672 | SPI-040853 | SPI-040853 | Truliant | EXACTECH, INC. | |
32 | 10885862605665 | SPI-040844 | SPI-040844 | Truliant | EXACTECH, INC. | |
33 | 10885862605542 | SPI-040738 | SPI-040738 | Truliant | EXACTECH, INC. | |
34 | 10885862603579 | SPI-040344 | SPI-040344 | Truliant | EXACTECH, INC. | |
35 | 10885862603562 | SPI-040343 | SPI-040343 | Truliant | EXACTECH, INC. | |
36 | 10885862603203 | SPI-040152 | SPI-040152 | Truliant | EXACTECH, INC. | |
37 | 10885862603128 | SPI-039661-60 | SPI-039661-60 | Truliant | EXACTECH, INC. | |
38 | 10885862603111 | SPI-039661-50 | SPI-039661-50 | Truliant | EXACTECH, INC. | |
39 | 10885862603104 | SPI-039661-45 | SPI-039661-45 | Truliant | EXACTECH, INC. | |
40 | 10885862603098 | SPI-039661-40 | SPI-039661-40 | Truliant | EXACTECH, INC. | |
41 | 10885862603081 | SPI-039661-35 | SPI-039661-35 | Truliant | EXACTECH, INC. | |
42 | 10885862603074 | SPI-039661-30 | SPI-039661-30 | Truliant | EXACTECH, INC. | |
43 | 10885862603067 | SPI-039661-25 | SPI-039661-25 | Truliant | EXACTECH, INC. | |
44 | 10885862603050 | SPI-039661-20 | SPI-039661-20 | Truliant | EXACTECH, INC. | |
45 | 10885862603043 | SPI-039661-15 | SPI-039661-15 | Truliant | EXACTECH, INC. | |
46 | 10885862603036 | SPI-039661-10 | SPI-039661-10 | Truliant | EXACTECH, INC. | |
47 | 10885862603029 | SPI-039661-00 | SPI-039661-00 | Truliant | EXACTECH, INC. | |
48 | 10885862603012 | SPI-039670-R | SPI-039670-R | Truliant | EXACTECH, INC. | |
49 | 10885862603005 | SPI-039670-L | SPI-039670-L | Truliant | EXACTECH, INC. | |
50 | 10885862602589 | SPI-039616 | SPI-039616 | Truliant | EXACTECH, INC. |