Other products from "TOTAL JOINT ORTHOPEDICS, INC."
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
Other products with the same Product Codes "MBH, 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
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.
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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.
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28 TKRL0000LL595 UKI0101-L UNIKO PointCloud™ Knee Instrument Kit Left PointCloud UNIK ORTHOPEDICS INC.
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42 TKRL0000FDFI5 UKI0101-L UNIKO PointCloud™ Knee Instrument Kit Left PointCloud UNIK ORTHOPEDICS INC.
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46 TKRL0000F5635 UKI0101-L UNIKO PointCloud™ Knee Instrument Kit Left PointCloud UNIK ORTHOPEDICS INC.
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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.
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