| No | Primary DI | Version or Model | Catalog Number | Device Description | Product Code | Product Code Name | Device Class | Brand Name |
|---|---|---|---|---|---|---|---|---|
| 1 | 07630345705761 | 02.12.10.1442 | Widget Size M - assembly | LXH | Orthopedic Manual Surgical Instrument | 1 | Knee Instruments | |
| 2 | 07630040789011 | 03.22.10.0070 | Assy Inner Shaft Short | LXH | Orthopedic Manual Surgical Instrument | 1 | Spine Instruments | |
| 3 | 07630040767033 | 02.02.10.0204 | Patellar palpator | LXH | Orthopedic Manual Surgical Instrument | 1 | Knee Instruments | |
| 4 | 07630040759137 | 02.07.10.3581 | Trial femur #1 Right | LXH | Orthopedic Manual Surgical Instrument | 1 | Knee Instruments | |
| 5 | 07630040754071 | 02.07.10.0532 | Caliper | LXH | Orthopedic Manual Surgical Instrument | 1 | Knee Instruments | |
| 6 | 07630040747493 | 01.26.10.0181 | Rod Posterior | LXH | Orthopedic Manual Surgical Instrument | 1 | Hip Instruments | |
| 7 | 07630040743686 | 01.10.10.337 | Long trocart | LXH | Orthopedic Manual Surgical Instrument | 1 | HIP Instruments | |
| 8 | 07630040717335 | 7.0706 | MySpine-MC vertebra S01 | PQC | Pedicle Screw Placement Guide | 2 | MySpine | |
| 9 | 07630030846519 | 3050.0024 | Inset Patella 24mm | JWH | Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer | 2 | Evolis Total Knee System | |
| 10 | 07630030834844 | 03.50.200 | Set screw (1x) Sterile | MNI,MNH,NKB,KWQ,KWP | Orthosis, Spinal Pedicle Fixation,Orthosis, Spondylolisthesis Spinal Fixation,Or Orthosis, Spinal Pedicle Fixation,Orthosis, Spondylolisthesis Spinal Fixation,Orthosis, Spinal Pedicle Fixation, For Degenerative Disc Disease,Appliance, Fixation, Spinal Intervertebral Body,Appliance, Fixation, Spinal Interlaminal | 2 | M.U.S.T. Set Screw | |
| 11 | 07630030806360 | 01.25.245M | Medacta Endo Head Ø 45, M | LZY | Prosthesis, Hip, Hemi-, Femoral, Metal Ball | 2 | Endohead | |
| 12 | 07630971243668 | 01.18.462 | AMIStem-P Short Neck STD stem #2 | LZO | Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented Or Non-Porous Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented Or Non-Porous, Uncemented | 2 | AMIStem-P Short Neck | |
| 13 | 07630971243651 | 01.18.461 | AMIStem-P Short Neck STD stem #1 | LZO | Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented Or Non-Porous Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented Or Non-Porous, Uncemented | 2 | AMIStem-P Short Neck | |
| 14 | 07630971282766 | 03.75.10.0125 | Poly-axial screwdriver_lockable | LXH | Orthopedic Manual Surgical Instrument | 1 | Spine Instruments | |
| 15 | 07630971281431 | 04.01.10.0522 | Modular Trephine – Graft Reamer | LXH | Orthopedic Manual Surgical Instrument | 1 | Shoulder Instruments | |
| 16 | 07630971231078 | 03.51.10.0263 | Pedicle Awl Sleek | LXH | Orthopedic Manual Surgical Instrument | 1 | Spine Instruments | |
| 17 | 07630971221079 | 03.75.10.0302 | Hook pusher | LXH | Orthopedic Manual Surgical Instrument | 1 | Spine Instruments | |
| 18 | 07630971210523 | 04.01.10.0116 | Intramedullary reamer - Ø8 - AO | LXH | Orthopedic Manual Surgical Instrument | 1 | Shoulder System Instrument | |
| 19 | 07630971209985 | 04.01.10.0040 | Reamer for glenosphere - Ø36 | LXH | Orthopedic Manual Surgical Instrument | 1 | Shoulder System Instrument | |
| 20 | 07630345780232 | 01.22.10.1379 | Monobloc L190-L240-L290 STD - LAT Template 110% | LXH | Orthopedic Manual Surgical Instrument | 1 | Hip Instruments | |
| 21 | 07630345737441 | 01.32.10.0555 | Inner rod for ref. 01.32.10.0554 | LXH | Orthopedic Manual Surgical Instrument | 1 | Hip Instruments | |
| 22 | 07630345737434 | 01.32.10.0554 | Cup impactor | LXH | Orthopedic Manual Surgical Instrument | 1 | Hip Instruments | |
| 23 | 07630345734488 | 03.75.10.0269 | MUST MINI connector sizer | LXH | Orthopedic Manual Surgical Instrument | 1 | Spine Instruments | |
| 24 | 07630345734457 | 03.51.10.0652 | Pin+Handweel for cannulated probe | LXH | Orthopedic Manual Surgical Instrument | 1 | Spine Instruments | |
| 25 | 07630345734440 | 03.51.10.0562 | Cannulated probe with spherical handle | LXH | Orthopedic Manual Surgical Instrument | 1 | Spine Instruments | |
| 26 | 07630345734389 | 01.10.10.220 | Femoral Head Extractor | LXH | Orthopedic Manual Surgical Instrument | 1 | Hip Instruments | |
| 27 | 07630345734136 | 03.51.10.0742 | Parallel compressor - long tip - deeper grooves | LXH | Orthopedic Manual Surgical Instrument | 1 | Spine Instruments | |
| 28 | 07630345734068 | 03.51.10.7431 | MUST MC Setscrewdriver Short RED Sleeve | LXH | Orthopedic Manual Surgical Instrument | 1 | Spine Instruments | |
| 29 | 07630345734051 | 03.51.10.7430 | MUST MC Setscrewdriver Short STD Sleeve | LXH | Orthopedic Manual Surgical Instrument | 1 | Spine Instruments | |
| 30 | 07630345734044 | 03.51.10.7429 | MUST MC Temporary Setscrewdriver Short | LXH | Orthopedic Manual Surgical Instrument | 1 | Spine Instruments | |
| 31 | 07630345734037 | 03.51.10.7428 | MUST MC Countertorque Short | LXH | Orthopedic Manual Surgical Instrument | 1 | Spine Instruments | |
| 32 | 07630345734020 | 03.51.10.7427 | MUST MC Countertorque | LXH | Orthopedic Manual Surgical Instrument | 1 | Spine Instruments | |
| 33 | 07630345734013 | 03.51.10.7426 | MUST MC Tab Remover | LXH | Orthopedic Manual Surgical Instrument | 1 | Spine Instruments | |
| 34 | 07630345734006 | 03.51.10.7425 | MUST MC Setscrewdriver RED Sleeve | LXH | Orthopedic Manual Surgical Instrument | 1 | Spine Instruments | |
| 35 | 07630345733993 | 03.51.10.7424 | MUST MC Setscrewdriver STD Sleeve | LXH | Orthopedic Manual Surgical Instrument | 1 | Spine Instruments | |
| 36 | 07630345733986 | 03.51.10.7423 | MUST MC Temporary Setscrewdriver | LXH | Orthopedic Manual Surgical Instrument | 1 | Spine Instruments | |
| 37 | 07630345733979 | 03.51.10.7422 | MUST MC Short Reducer | LXH | Orthopedic Manual Surgical Instrument | 1 | Spine Instruments | |
| 38 | 07630345733962 | 03.51.10.7421 | MUST MC Gradual Persuader | LXH | Orthopedic Manual Surgical Instrument | 1 | Spine Instruments | |
| 39 | 07630345733955 | 03.51.10.7420 | MUST MC One Step Reducer | LXH | Orthopedic Manual Surgical Instrument | 1 | Spine Instruments | |
| 40 | 07630345733948 | 03.51.10.7419 | MUST MC Rod Forceps | LXH | Orthopedic Manual Surgical Instrument | 1 | Spine Instruments | |
| 41 | 07630345733931 | 03.51.10.7418 | MUST MC Head Adjuster | LXH | Orthopedic Manual Surgical Instrument | 1 | Spine Instruments | |
| 42 | 07630345733924 | 03.51.10.7417 | MUST MC Pedicle Screwdriver Sleeve RED | LXH | Orthopedic Manual Surgical Instrument | 1 | Spine Instruments | |
| 43 | 07630345733917 | 03.51.10.7416 | MUST MC Pedicle Screwdriver Sleeve STD | LXH | Orthopedic Manual Surgical Instrument | 1 | Spine Instruments | |
| 44 | 07630345733900 | 03.51.10.7415 | MUST MC Pedicle Screwdriver – Outer Sleeve | LXH | Orthopedic Manual Surgical Instrument | 1 | Spine Instruments | |
| 45 | 07630345733894 | 03.51.10.7414 | MUST MC Pedicle Screwdriver – Shaft | LXH | Orthopedic Manual Surgical Instrument | 1 | Spine Instruments | |
| 46 | 07630345733887 | 03.51.10.7413 | MUST MC 4 Leads Taps Inline Solid Ø7 | LXH | Orthopedic Manual Surgical Instrument | 1 | Spine Instruments | |
| 47 | 07630345733870 | 03.51.10.7412 | MUST MC 4 Leads Taps Inline Solid Ø6.5 | LXH | Orthopedic Manual Surgical Instrument | 1 | Spine Instruments | |
| 48 | 07630345733863 | 03.51.10.7411 | MUST MC 4 Leads Taps Inline Solid Ø6 | LXH | Orthopedic Manual Surgical Instrument | 1 | Spine Instruments | |
| 49 | 07630040723398 | 05.05.0005 | Interference Screw 6x25 T20 | MBI | Fastener, Fixation, Nondegradable, Soft Tissue | 2 | MectaScrew PEEK | |
| 50 | 07630345733856 | 03.51.10.7410 | MUST MC 4 Leads Taps Inline Solid Ø5.5 | LXH | Orthopedic Manual Surgical Instrument | 1 | Spine Instruments |
| 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. |