Other products from "RESPONSIVE ORTHOPEDICS, LLC"
No Primary DI Version or Model Catalog Number Device Description Product Code Product Code Name Device Class Brand Name
1 00841973106937 90-SRK-180218 90-SRK-180218 TRIAL 90-SRK-180218 POLY PS 2X18MM JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer 2 Responsive Orthopedics Total Knee Arthroplasty System
2 00841973106920 90-SRK-180216 90-SRK-180216 TRIAL 90-SRK-180216 POLY PS 2X16MM JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer 2 Responsive Orthopedics Total Knee Arthroplasty System
3 00841973106913 90-SRK-180214 90-SRK-180214 TRIAL 90-SRK-180214 POLY PS 2X14MM JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer 2 Responsive Orthopedics Total Knee Arthroplasty System
4 00841973106906 90-SRK-180212 90-SRK-180212 TRIAL 90-SRK-180212 POLY PS 2X12MM JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer 2 Responsive Orthopedics Total Knee Arthroplasty System
5 00841973106890 90-SRK-180210 90-SRK-180210 TRIAL 90-SRK-180210 POLY PS 2X10MM JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer 2 Responsive Orthopedics Total Knee Arthroplasty System
6 00841973106883 90-SRK-180120 90-SRK-180120 TRIAL 90-SRK-180120 POLY PS 1X20MM JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer 2 Responsive Orthopedics Total Knee Arthroplasty System
7 00841973106876 90-SRK-180118 90-SRK-180118 TRIAL 90-SRK-180118 POLY PS 1X18MM JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer 2 Responsive Orthopedics Total Knee Arthroplasty System
8 00841973106869 90-SRK-180116 90-SRK-180116 TRIAL 90-SRK-180116 POLY PS 1X16MM JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer 2 Responsive Orthopedics Total Knee Arthroplasty System
9 00841973106852 90-SRK-180114 90-SRK-180114 TRIAL 90-SRK-180114 POLY PS 1X14MM JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer 2 Responsive Orthopedics Total Knee Arthroplasty System
10 00841973106845 90-SRK-180112 90-SRK-180112 TRIAL 90-SRK-180112 POLY PS 1X12MM JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer 2 Responsive Orthopedics Total Knee Arthroplasty System
11 00841973106838 90-SRK-180110 90-SRK-180110 TRIAL 90-SRK-180110 POLY PS 1X10MM JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer 2 Responsive Orthopedics Total Knee Arthroplasty System
12 00841973106821 90-SRK-353126 90-SRK-353126 TRIAL 90-SRK-353126 PS FEMORAL 6 LEFT JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer 2 Responsive Orthopedics Total Knee Arthroplasty System
13 00841973106814 90-SRK-353125 90-SRK-353125 TRIAL 90-SRK-353125 PS FEMORAL 5 LEFT JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer 2 Responsive Orthopedics Total Knee Arthroplasty System
14 00841973101703 90-SRK-142314 Poly Insert MPCS, Size 3L, 14mm JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer 2 Responsive Orthopedics Total Knee Arthroplasty System
15 00841973106807 90-SRK-353124 90-SRK-353124 TRIAL 90-SRK-353124 PS FEMORAL 4 LEFT JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer 2 Responsive Orthopedics Total Knee Arthroplasty System
16 00841973106791 90-SRK-353123 90-SRK-353123 TRIAL 90-SRK-353123 PS FEMORAL 3 LEFT JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer 2 Responsive Orthopedics Total Knee Arthroplasty System
17 00841973106784 90-SRK-353122 90-SRK-353122 TRIAL 90-SRK-353122 PS FEMORAL 2 LEFT JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer 2 Responsive Orthopedics Total Knee Arthroplasty System
18 00841973106777 90-SRK-353121 90-SRK-353121 TRIAL 90-SRK-353121 PS FEMORAL 1 LEFT JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer 2 Responsive Orthopedics Total Knee Arthroplasty System
19 00841973106760 90-SRK-353116 90-SRK-353116 TRIAL 90-SRK-353116 PS FEMORAL 6 RIGHT JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer 2 Responsive Orthopedics Total Knee Arthroplasty System
20 00841973106753 90-SRK-353115 90-SRK-353115 TRIAL 90-SRK-353115 PS FEMORAL 5 RIGHT JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer 2 Responsive Orthopedics Total Knee Arthroplasty System
21 00841973106746 90-SRK-353114 90-SRK-353114 TRIAL 90-SRK-353114 PS FEMORAL 4 RIGHT JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer 2 Responsive Orthopedics Total Knee Arthroplasty System
22 00841973106739 90-SRK-353113 90-SRK-353113 TRIAL 90-SRK-353113 PS FEMORAL 3 RIGHT JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer 2 Responsive Orthopedics Total Knee Arthroplasty System
23 00841973106722 90-SRK-353112 90-SRK-353112 TRIAL 90-SRK-353112 PS FEMORAL 2 RIGHT JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer 2 Responsive Orthopedics Total Knee Arthroplasty System
24 00841973106715 90-SRK-353111 90-SRK-353111 TRIAL 90-SRK-353111 PS FEMORAL 1 RIGHT JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer 2 Responsive Orthopedics Total Knee Arthroplasty System
25 00841973101697 90-SRK-142312 Poly Insert MPCS, Size 3L, 12mm JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer 2 Responsive Orthopedics Total Knee Arthroplasty System
26 00841973106708 90-SRK-160620 90-SRK-160620 TRIAL 90-SRK-160620 POLY CR 6X20MM JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer 2 Responsive Orthopedics Total Knee Arthroplasty System
27 00841973106692 90-SRK-160618 90-SRK-160618 TRIAL 90-SRK-160618 POLY CR 6X18MM JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer 2 Responsive Orthopedics Total Knee Arthroplasty System
28 00841973106685 90-SRK-160616 90-SRK-160616 TRIAL 90-SRK-160616 POLY CR 6X16MM JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer 2 Responsive Orthopedics Total Knee Arthroplasty System
29 00841973106678 90-SRK-160614 90-SRK-160614 TRIAL 90-SRK-160614 POLY CR 6X14MM JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer 2 Responsive Orthopedics Total Knee Arthroplasty System
30 00841973106661 90-SRK-160612 90-SRK-160612 TRIAL 90-SRK-160612 POLY CR 6X12MM JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer 2 Responsive Orthopedics Total Knee Arthroplasty System
31 00841973106654 90-SRK-160610 90-SRK-160610 TRIAL 90-SRK-160610 POLY CR 6X10MM JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer 2 Responsive Orthopedics Total Knee Arthroplasty System
32 00841973106647 90-SRK-160520 90-SRK-160520 TRIAL 90-SRK-160520 POLY CR 5X20MM JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer 2 Responsive Orthopedics Total Knee Arthroplasty System
33 00841973106630 90-SRK-160518 90-SRK-160518 TRIAL 90-SRK-160518 POLY CR 5X18MM JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer 2 Responsive Orthopedics Total Knee Arthroplasty System
34 00841973106623 90-SRK-160516 90-SRK-160516 TRIAL 90-SRK-160516 POLY CR 5X16MM JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer 2 Responsive Orthopedics Total Knee Arthroplasty System
35 00841973106616 90-SRK-160514 90-SRK-160514 TRIAL 90-SRK-160514 POLY CR 5X14MM JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer 2 Responsive Orthopedics Total Knee Arthroplasty System
36 00841973101680 90-SRK-142310 Poly Insert MPCS, Size 3L, 10mm JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer 2 Responsive Orthopedics Total Knee Arthroplasty System
37 00841973106609 90-SRK-160512 90-SRK-160512 TRIAL 90-SRK-160512 POLY CR 5X12MM JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer 2 Responsive Orthopedics Total Knee Arthroplasty System
38 00841973106593 90-SRK-160510 90-SRK-160510 TRIAL 90-SRK-160510 POLY CR 5X10MM JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer 2 Responsive Orthopedics Total Knee Arthroplasty System
39 00841973106586 90-SRK-160420 90-SRK-160420 TRIAL 90-SRK-160420 POLY CR 4X20MM JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer 2 Responsive Orthopedics Total Knee Arthroplasty System
40 00841973106579 90-SRK-160418 90-SRK-160418 TRIAL 90-SRK-160418 POLY CR 4X18MM JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer 2 Responsive Orthopedics Total Knee Arthroplasty System
41 00841973106562 90-SRK-160416 90-SRK-160416 TRIAL 90-SRK-160416 POLY CR 4X16MM JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer 2 Responsive Orthopedics Total Knee Arthroplasty System
42 00841973106555 90-SRK-160414 90-SRK-160414 TRIAL 90-SRK-160414 POLY CR 4X14MM JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer 2 Responsive Orthopedics Total Knee Arthroplasty System
43 00841973106548 90-SRK-160412 90-SRK-160412 TRIAL 90-SRK-160412 POLY CR 4X12MM JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer 2 Responsive Orthopedics Total Knee Arthroplasty System
44 00841973106531 90-SRK-160410 90-SRK-160410 TRIAL 90-SRK-160410 POLY CR 4X10MM JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer 2 Responsive Orthopedics Total Knee Arthroplasty System
45 00841973106524 90-SRK-160320 90-SRK-160320 TRIAL 90-SRK-160320 POLY CR 3X20MM JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer 2 Responsive Orthopedics Total Knee Arthroplasty System
46 00841973106517 90-SRK-160318 90-SRK-160318 TRIAL 90-SRK-160318 POLY CR 3X18MM JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer 2 Responsive Orthopedics Total Knee Arthroplasty System
47 00841973106500 90-SRK-160316 90-SRK-160316 TRIAL 90-SRK-160316 POLY CR 3X16MM JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer 2 Responsive Orthopedics Total Knee Arthroplasty System
48 00841973106494 90-SRK-160314 90-SRK-160314 TRIAL 90-SRK-160314 POLY CR 3X14MM JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer 2 Responsive Orthopedics Total Knee Arthroplasty System
49 00841973106487 90-SRK-160312 90-SRK-160312 TRIAL 90-SRK-160312 POLY CR 3X12MM JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer 2 Responsive Orthopedics Total Knee Arthroplasty System
50 00841973106470 90-SRK-160310 90-SRK-160310 TRIAL 90-SRK-160310 POLY CR 3X10MM JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer 2 Responsive Orthopedics Total Knee Arthroplasty System
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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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.
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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.
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38 10885862603111 SPI-039661-50 SPI-039661-50 Truliant EXACTECH, INC.
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