No | Primary DI | Version or Model | Catalog Number | Device Description | Product Code | Product Code Name | Device Class | Brand Name |
---|---|---|---|---|---|---|---|---|
1 | 00819251029575 | 2254.06.024 | Tibial Insert Trial,PS-Post, size 6, 24mm | LXH | Orthopedic manual surgical instrument | 1 | Tibial Insert Trial, PS-Post, Klassic ONE | |
2 | 00819251029568 | 2254.06.021 | Tibial Insert Trial,PS-Post, size 6, 21mm | LXH | Orthopedic manual surgical instrument | 1 | Tibial Insert Trial, PS-Post, Klassic ONE | |
3 | 00819251029551 | 2254.06.018 | Tibial Insert Trial,PS-Post, size 6, 18mm | LXH | Orthopedic manual surgical instrument | 1 | Tibial Insert Trial, PS-Post, Klassic ONE | |
4 | 00819251029544 | 2254.05.024 | Tibial Insert Trial,PS-Post, size 5, 24mm | LXH | Orthopedic manual surgical instrument | 1 | Tibial Insert Trial, PS-Post, Klassic ONE | |
5 | 00819251029537 | 2254.05.021 | Tibial Insert Trial,PS-Post, size 5, 21mm | LXH | Orthopedic manual surgical instrument | 1 | Tibial Insert Trial, PS-Post, Klassic ONE | |
6 | 00819251029520 | 2254.05.018 | Tibial Insert Trial,PS-Post, size 5, 18mm | LXH | Orthopedic manual surgical instrument | 1 | Tibial Insert Trial, PS-Post, Klassic ONE | |
7 | 00819251029513 | 2254.04.024 | Tibial Insert Trial,PS-Post, size 4, 24mm | LXH | Orthopedic manual surgical instrument | 1 | Tibial Insert Trial, PS-Post, Klassic ONE | |
8 | 00819251029506 | 2254.04.021 | Tibial Insert Trial,PS-Post, size 4, 21mm | LXH | Orthopedic manual surgical instrument | 1 | Tibial Insert Trial, PS-Post, Klassic ONE | |
9 | 00819251029490 | 2254.04.018 | Tibial Insert Trial,PS-Post, size 4, 18mm | LXH | Orthopedic manual surgical instrument | 1 | Tibial Insert Trial, PS-Post, Klassic ONE | |
10 | 00819251029483 | 2254.03.024 | Tibial Insert Trial,PS-Post, size 3, 24mm | LXH | Orthopedic manual surgical instrument | 1 | Tibial Insert Trial, PS-Post, Klassic ONE | |
11 | 00819251029476 | 2254.03.021 | Tibial Insert Trial,PS-Post, size 3, 21mm | LXH | Orthopedic manual surgical instrument | 1 | Tibial Insert Trial, PS-Post, Klassic ONE | |
12 | 00819251029469 | 2254.03.018 | Tibial Insert Trial,PS-Post, size 3, 18mm | LXH | Orthopedic manual surgical instrument | 1 | Tibial Insert Trial, PS-Post, Klassic ONE | |
13 | 00819251029452 | 2254.02.024 | Tibial Insert Trial,PS-Post, size 2, 24mm | LXH | Orthopedic manual surgical instrument | 1 | Tibial Insert Trial, PS-Post, Klassic ONE | |
14 | 00819251029445 | 2254.02.021 | Tibial Insert Trial,PS-Post, size 2, 21mm | LXH | Orthopedic manual surgical instrument | 1 | Tibial Insert Trial, PS-Post, Klassic ONE | |
15 | 00819251029438 | 2254.02.018 | Tibial Insert Trial,PS-Post, size 2, 18mm | LXH | Orthopedic manual surgical instrument | 1 | Tibial Insert Trial, PS-Post, Klassic ONE | |
16 | 00819251029421 | 2254.01.024 | Tibial Insert Trial,PS-Post, size 1, 24mm | LXH | Orthopedic manual surgical instrument | 1 | Tibial Insert Trial, PS-Post, Klassic ONE | |
17 | 00819251029414 | 2254.01.021 | Tibial Insert Trial,PS-Post, size 1, 21mm | LXH | Orthopedic manual surgical instrument | 1 | Tibial Insert Trial, PS-Post, Klassic ONE | |
18 | 00819251029407 | 2254.01.018 | Tibial Insert Trial,PS-Post, size 1, 18mm | LXH | Orthopedic manual surgical instrument | 1 | Tibial Insert Trial, PS-Post, Klassic ONE | |
19 | 00819251029247 | 1346.36.105 | Femoral Head Trial, 36mm, +10.5mm head length | LXH | Orthopedic manual surgical instrument | 1 | Klassic Femoral Head Trial | |
20 | 00819251029230 | 1346.32.105 | Femoral Head Trial, 32mm, +10.5mm head length | LXH | Orthopedic manual surgical instrument | 1 | Klassic Femoral Head Trial | |
21 | 00819251027687 | 2245.05.000 | All-Poly Tibial Broach, Size 5-6 | LXH | ORTHOPEDIC MANUAL SURGICAL INSTRUMENT | 1 | All-Poly Tibial Broach, Klassic ONE | |
22 | 00819251027670 | 2245.03.000 | All-Poly Tibial Broach, Size 3-4 | LXH | ORTHOPEDIC MANUAL SURGICAL INSTRUMENT | 1 | All-Poly Tibial Broach, Klassic ONE | |
23 | 00819251027663 | 2245.01.000 | All-Poly Tibial Broach, Size 1-2 | LXH | ORTHOPEDIC MANUAL SURGICAL INSTRUMENT | 1 | All-Poly Tibial Broach, Klassic ONE | |
24 | 00819251026932 | 2249.00.000 | Tibial Alignment Guide, 3 degrees Upper Tower | LXH | ORTHOPEDIC MANUAL SURGICAL INSTRUMENT | 1 | Tibial Alignment Guide, Upper Tower, Klassic ONE | |
25 | 00819251026925 | 2248.00.000 | Tibial Alignment Guide, 0 degree Upper Tower | LXH | ORTHOPEDIC MANUAL SURGICAL INSTRUMENT | 1 | Tibial Alignment Guide, Upper Tower, Klassic ONE | |
26 | 00819251026901 | 2254.06.016 | Tibial Insert Trial,PS-Post, size 6, 16mm | LXH | ORTHOPEDIC MANUAL SURGICAL INSTRUMENT | 1 | Tibial Insert Trial, PS-Post, Klassic ONE | |
27 | 00819251026895 | 2254.06.014 | Tibial Insert Trial,PS-Post, size 6, 14mm | LXH | ORTHOPEDIC MANUAL SURGICAL INSTRUMENT | 1 | Tibial Insert Trial, PS-Post, Klassic ONE | |
28 | 00819251026888 | 2254.06.013 | Tibial Insert Trial,PS-Post, size 6, 13mm | LXH | ORTHOPEDIC MANUAL SURGICAL INSTRUMENT | 1 | Tibial Insert Trial, PS-Post, Klassic ONE | |
29 | 00819251026871 | 2254.06.012 | Tibial Insert Trial,PS-Post, size 6, 12mm | LXH | ORTHOPEDIC MANUAL SURGICAL INSTRUMENT | 1 | Tibial Insert Trial, PS-Post, Klassic ONE | |
30 | 00819251026864 | 2254.06.011 | Tibial Insert Trial,PS-Post, size 6, 11mm | LXH | ORTHOPEDIC MANUAL SURGICAL INSTRUMENT | 1 | Tibial Insert Trial, PS-Post, Klassic ONE | |
31 | 00819251026857 | 2254.06.010 | Tibial Insert Trial,PS-Post, size 6, 10mm | LXH | ORTHOPEDIC MANUAL SURGICAL INSTRUMENT | 1 | Tibial Insert Trial, PS-Post, Klassic ONE | |
32 | 00819251026840 | 2254.05.016 | Tibial Insert Trial,PS-Post, size 5, 16mm | LXH | ORTHOPEDIC MANUAL SURGICAL INSTRUMENT | 1 | Tibial Insert Trial, PS-Post, Klassic ONE | |
33 | 00819251026833 | 2254.05.014 | Tibial Insert Trial,PS-Post, size 5, 14mm | LXH | ORTHOPEDIC MANUAL SURGICAL INSTRUMENT | 1 | Tibial Insert Trial, PS-Post, Klassic ONE | |
34 | 00819251026826 | 2254.05.013 | Tibial Insert Trial,PS-Post, size 5, 13mm | LXH | ORTHOPEDIC MANUAL SURGICAL INSTRUMENT | 1 | Tibial Insert Trial, PS-Post, Klassic ONE | |
35 | 00819251026819 | 2254.05.012 | Tibial Insert Trial,PS-Post, size 5, 12mm | LXH | ORTHOPEDIC MANUAL SURGICAL INSTRUMENT | 1 | Tibial Insert Trial, PS-Post, Klassic ONE | |
36 | 00819251026802 | 2254.05.011 | Tibial Insert Trial,PS-Post, size 5, 11mm | LXH | ORTHOPEDIC MANUAL SURGICAL INSTRUMENT | 1 | Tibial Insert Trial, PS-Post, Klassic ONE | |
37 | 00819251026796 | 2254.05.010 | Tibial Insert Trial,PS-Post, size 5, 10mm | LXH | ORTHOPEDIC MANUAL SURGICAL INSTRUMENT | 1 | Tibial Insert Trial, PS-Post, Klassic ONE | |
38 | 00819251026789 | 2254.04.016 | Tibial Insert Trial,PS-Post, size 4, 16mm | LXH | ORTHOPEDIC MANUAL SURGICAL INSTRUMENT | 1 | Tibial Insert Trial, PS-Post, Klassic ONE | |
39 | 00819251026772 | 2254.04.014 | Tibial Insert Trial,PS-Post, size 4, 14mm | LXH | ORTHOPEDIC MANUAL SURGICAL INSTRUMENT | 1 | Tibial Insert Trial, PS-Post, Klassic ONE | |
40 | 00819251026765 | 2254.04.013 | Tibial Insert Trial,PS-Post, size 4, 13mm | LXH | ORTHOPEDIC MANUAL SURGICAL INSTRUMENT | 1 | Tibial Insert Trial, PS-Post, Klassic ONE | |
41 | 00819251026758 | 2254.04.012 | Tibial Insert Trial,PS-Post, size 4, 12mm | LXH | ORTHOPEDIC MANUAL SURGICAL INSTRUMENT | 1 | Tibial Insert Trial, PS-Post, Klassic ONE | |
42 | 00819251026741 | 2254.04.011 | Tibial Insert Trial,PS-Post, size 4, 11mm | LXH | ORTHOPEDIC MANUAL SURGICAL INSTRUMENT | 1 | Tibial Insert Trial, PS-Post, Klassic ONE | |
43 | 00819251026734 | 2254.04.010 | Tibial Insert Trial,PS-Post, size 4, 10mm | LXH | ORTHOPEDIC MANUAL SURGICAL INSTRUMENT | 1 | Tibial Insert Trial, PS-Post, Klassic ONE | |
44 | 00819251026727 | 2254.03.016 | Tibial Insert Trial,PS-Post, size 3, 16mm | LXH | ORTHOPEDIC MANUAL SURGICAL INSTRUMENT | 1 | Tibial Insert Trial, PS-Post, Klassic ONE | |
45 | 00819251026710 | 2254.03.014 | Tibial Insert Trial,PS-Post, size 3, 14mm | LXH | ORTHOPEDIC MANUAL SURGICAL INSTRUMENT | 1 | Tibial Insert Trial, PS-Post, Klassic ONE | |
46 | 00819251026703 | 2254.03.013 | Tibial Insert Trial,PS-Post, size 3, 13mm | LXH | ORTHOPEDIC MANUAL SURGICAL INSTRUMENT | 1 | Tibial Insert Trial, PS-Post, Klassic ONE | |
47 | 00819251026697 | 2254.03.012 | Tibial Insert Trial,PS-Post, size 3, 12mm | LXH | ORTHOPEDIC MANUAL SURGICAL INSTRUMENT | 1 | Tibial Insert Trial, PS-Post, Klassic ONE | |
48 | 00819251026680 | 2254.03.011 | Tibial Insert Trial,PS-Post, size 3, 11mm | LXH | ORTHOPEDIC MANUAL SURGICAL INSTRUMENT | 1 | Tibial Insert Trial, PS-Post, Klassic ONE | |
49 | 00819251026673 | 2254.03.010 | Tibial Insert Trial,PS-Post, size 3, 10mm | LXH | ORTHOPEDIC MANUAL SURGICAL INSTRUMENT | 1 | Tibial Insert Trial, PS-Post, Klassic ONE | |
50 | 00819251026666 | 2254.02.016 | Tibial Insert Trial,PS-Post, size 2, 16mm | LXH | ORTHOPEDIC MANUAL SURGICAL INSTRUMENT | 1 | Tibial Insert Trial, PS-Post, Klassic ONE |
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 | TKRR0000LLBL5 | UKI0101-R | UNIKO PointCloud™ Knee Instrument Kit Right | PointCloud | UNIK ORTHOPEDICS INC. | |
10 | TKRR0000LID65 | UKI0101-R | UNIKO PointCloud™ Knee Instrument Kit Right | PointCloud | UNIK ORTHOPEDICS INC. | |
11 | TKRR0000LI745 | UKI0101-R | UNIKO PointCloud™ Knee Instrument Kit Right | PointCloud | UNIK ORTHOPEDICS INC. | |
12 | TKRR0000LI105 | UKI0101-R | UNIKO PointCloud™ Knee Instrument Kit Right | PointCloud | UNIK ORTHOPEDICS INC. | |
13 | TKRR0000LD2D5 | UKI0101-R | UNIKO PointCloud™ Knee Instrument Kit Right | PointCloud | UNIK ORTHOPEDICS INC. | |
14 | TKRR0000LB3B5 | UKI0101-R | UNIKO PointCloud™ Knee Instrument Kit Right | PointCloud | UNIK ORTHOPEDICS INC. | |
15 | TKRR0000L6855 | UKI0101-R | UNIKO PointCloud™ Knee Instrument Kit Right | PointCloud | UNIK ORTHOPEDICS INC. | |
16 | TKRR0000L6265 | UKI0101-R | UNIKO PointCloud™ Knee Instrument Kit Right | PointCloud | UNIK ORTHOPEDICS INC. | |
17 | TKRR0000L5K05 | UKI0101-R | UNIKO PointCloud™ Knee Instrument Kit Right | PointCloud | UNIK ORTHOPEDICS INC. | |
18 | TKRR0000L4F85 | UKI0101-R | UNIKO PointCloud™ Knee Instrument Kit Right | PointCloud | UNIK ORTHOPEDICS INC. | |
19 | TKRR0000FK065 | UKI0101-R | UNIKO PointCloud™ Knee Instrument Kit Right | PointCloud | UNIK ORTHOPEDICS INC. | |
20 | TKRR0000FI7I5 | UKI0101-R | UNIKO PointCloud™ Knee Instrument Kit Right | PointCloud | UNIK ORTHOPEDICS INC. | |
21 | TKRR0000FF8D5 | UKI0101-R | UNIKO PointCloud™ Knee Instrument Kit Right | PointCloud | UNIK ORTHOPEDICS INC. | |
22 | TKRR0000FF295 | UKI0101-R | UNIKO PointCloud™ Knee Instrument Kit Right | PointCloud | UNIK ORTHOPEDICS INC. | |
23 | TKRR0000FB3F5 | UKI0101-R | UNIKO PointCloud™ Knee Instrument Kit Right | PointCloud | UNIK ORTHOPEDICS INC. | |
24 | TKRR0000F4995 | UKI0101-R | UNIKO PointCloud™ Knee Instrument Kit Right | PointCloud | UNIK ORTHOPEDICS INC. | |
25 | TKRR0000F17L5 | UKI0101-R | UNIKO PointCloud™ Knee Instrument Kit Right | PointCloud | UNIK ORTHOPEDICS INC. | |
26 | TKRR0000DFL65 | UKI0101-R | UNIKO PointCloud™ Knee Instrument Kit Right | PointCloud | UNIK ORTHOPEDICS INC. | |
27 | TKRR0000DF825 | UKI0101-R | UNIKO PointCloud™ Knee Instrument Kit Right | PointCloud | UNIK ORTHOPEDICS INC. | |
28 | TKRL0000LL595 | UKI0101-L | UNIKO PointCloud™ Knee Instrument Kit Left | PointCloud | UNIK ORTHOPEDICS INC. | |
29 | TKRL0000LK015 | UKI0101-L | UNIKO PointCloud™ Knee Instrument Kit Left | PointCloud | UNIK ORTHOPEDICS INC. | |
30 | TKRL0000LF225 | UKI0101-L | UNIKO PointCloud™ Knee Instrument Kit Left | PointCloud | UNIK ORTHOPEDICS INC. | |
31 | TKRL0000LDF45 | UKI0101-L | UNIKO PointCloud™ Knee Instrument Kit Left | PointCloud | UNIK ORTHOPEDICS INC. | |
32 | TKRL0000LBI35 | UKI0101-L | UNIKO PointCloud™ Knee Instrument Kit Left | PointCloud | UNIK ORTHOPEDICS INC. | |
33 | TKRL0000L6F15 | UKI0101-L | UNIKO PointCloud™ Knee Instrument Kit Left | PointCloud | UNIK ORTHOPEDICS INC. | |
34 | TKRL0000L55K5 | UKI0101-L | UNIKO PointCloud™ Knee Instrument Kit Left | PointCloud | UNIK ORTHOPEDICS INC. | |
35 | TKRL0000L3D05 | UKI0101-L | UNIKO PointCloud™ Knee Instrument Kit Left | PointCloud | UNIK ORTHOPEDICS INC. | |
36 | TKRL0000FLK35 | UKI0101-L | UNIKO PointCloud™ Knee Instrument Kit Left | PointCloud | UNIK ORTHOPEDICS INC. | |
37 | TKRL0000FKD15 | UKI0101-L | UNIKO PointCloud™ Knee Instrument Kit Left | PointCloud | UNIK ORTHOPEDICS INC. | |
38 | TKRL0000FK6D5 | UKI0101-L | UNIKO PointCloud™ Knee Instrument Kit Left | PointCloud | UNIK ORTHOPEDICS INC. | |
39 | TKRL0000FID95 | UKI0101-L | UNIKO PointCloud™ Knee Instrument Kit Left | PointCloud | UNIK ORTHOPEDICS INC. | |
40 | TKRL0000FI105 | UKI0101-L | UNIKO PointCloud™ Knee Instrument Kit Left | PointCloud | UNIK ORTHOPEDICS INC. | |
41 | TKRL0000FFLL5 | UKI0101-L | UNIKO PointCloud™ Knee Instrument Kit Left | PointCloud | UNIK ORTHOPEDICS INC. | |
42 | TKRL0000FDFI5 | UKI0101-L | UNIKO PointCloud™ Knee Instrument Kit Left | PointCloud | UNIK ORTHOPEDICS INC. | |
43 | TKRL0000FD945 | UKI0101-L | UNIKO PointCloud™ Knee Instrument Kit Left | PointCloud | UNIK ORTHOPEDICS INC. | |
44 | TKRL0000FD355 | UKI0101-L | UNIKO PointCloud™ Knee Instrument Kit Left | PointCloud | UNIK ORTHOPEDICS INC. | |
45 | TKRL0000F8845 | UKI0101-L | UNIKO PointCloud™ Knee Instrument Kit Left | PointCloud | UNIK ORTHOPEDICS INC. | |
46 | TKRL0000F5635 | UKI0101-L | UNIKO PointCloud™ Knee Instrument Kit Left | PointCloud | UNIK ORTHOPEDICS INC. | |
47 | TKRL0000F30I5 | UKI0101-L | UNIKO PointCloud™ Knee Instrument Kit Left | PointCloud | UNIK ORTHOPEDICS INC. | |
48 | TKRL0000F1L25 | UKI0101-L | UNIKO PointCloud™ Knee Instrument Kit Left | PointCloud | UNIK ORTHOPEDICS INC. | |
49 | 10885862621931 | SPI-046699 | SPI-046699 | Special Pinned Femoral RT- INT/ LT-EXT Rotation Adjustment Block | Truliant | EXACTECH, INC. |
50 | 10885862621924 | SPI-046300 | SPI-046300 | Special Pinned Femoral LT-INT / RT- EXT Rotation Adjustment Block | Truliant | EXACTECH, INC. |