Other products from "ZIMMER TRABECULAR METAL TECHNOLOGY INC."
No Primary DI Version or Model Catalog Number Device Description Product Code Product Code Name Device Class Brand Name
1 00889024464315 00-7050-078-00 FSM TRAY, SURGICAL, INSTRUMENT 1 NA
2 00889024464292 00-7050-076-00 FSM TRAY, SURGICAL, INSTRUMENT 1 NA
3 00889024464278 00-7050-038-00 HWR DRIVER, PROSTHESIS 1 NA
4 00889024464261 00-7050-036-00 HWR DRIVER, PROSTHESIS 1 NA
5 00889024464254 00-7361-052-22 HXB PROBE 1 NA
6 00889024464247 00-7360-070-28 HXB PROBE 1 NA
7 00889024464230 00-7360-068-28 HXB PROBE 1 NA
8 00889024464223 00-7360-066-28 HXB PROBE 1 NA
9 00889024464216 00-7360-064-28 HXB PROBE 1 NA
10 00889024464209 00-7360-062-28 HXB PROBE 1 NA
11 00889024464193 00-7360-060-28 HXB PROBE 1 NA
12 00889024464186 00-7360-058-28 HXB PROBE 1 NA
13 00889024464179 00-7360-056-28 HXB PROBE 1 NA
14 00889024464162 00-7360-054-28 HXB PROBE 1 NA
15 00889024464155 00-7360-052-28 HXB PROBE 1 NA
16 00889024320635 96-701-30001 MAX,GAD Intervertebral fusion device with bone graft, lumbar,RETRACTOR 1 TM Ardis®
17 00889024320628 96-701-21161 96-701-21161 GAD,MAX RETRACTOR,Intervertebral fusion device with bone graft, lumbar 1 TM Ardis®
18 00889024320611 96-701-21121 GAD,MAX RETRACTOR,Intervertebral fusion device with bone graft, lumbar 1 TM Ardis®
19 00889024320604 96-701-21101 GAD,MAX RETRACTOR,Intervertebral fusion device with bone graft, lumbar 1 TM Ardis®
20 00889024320598 96-701-21081 96-701-21081 GAD,MAX RETRACTOR,Intervertebral fusion device with bone graft, lumbar 1 TM Ardis®
21 00889024320581 96-701-20161 MAX,GAD Intervertebral fusion device with bone graft, lumbar,RETRACTOR 1 TM Ardis®
22 00889024320574 96-701-20121 96-701-20121 MAX,GAD Intervertebral fusion device with bone graft, lumbar,RETRACTOR 1 TM Ardis®
23 00889024320567 96-701-20101 96-701-20101 MAX,GAD Intervertebral fusion device with bone graft, lumbar,RETRACTOR 1 TM Ardis®
24 00889024320550 96-701-20081 MAX,GAD Intervertebral fusion device with bone graft, lumbar,RETRACTOR 1 TM Ardis®
25 00889024320543 96-701-10001 96-701-10001 MAX Intervertebral fusion device with bone graft, lumbar 2 TM Ardis®
26 00889024320536 96-499-60001 96-499-60001 FSM,MQP,MAX TRAY, SURGICAL, INSTRUMENT,SPINAL VERTEBRAL BODY REPLACEMENT DEVICE,Intervertebr TRAY, SURGICAL, INSTRUMENT,SPINAL VERTEBRAL BODY REPLACEMENT DEVICE,Intervertebral fusion device with bone graft, lumbar 1 NA
27 00889024320529 96-499-50001 96-499-50001 MQP,MAX,FSM SPINAL VERTEBRAL BODY REPLACEMENT DEVICE,Intervertebral fusion device with bone SPINAL VERTEBRAL BODY REPLACEMENT DEVICE,Intervertebral fusion device with bone graft, lumbar,TRAY, SURGICAL, INSTRUMENT 1 NA
28 00889024320512 96-499-40001 96-499-40001 MQP,MAX,FSM SPINAL VERTEBRAL BODY REPLACEMENT DEVICE,Intervertebral fusion device with bone SPINAL VERTEBRAL BODY REPLACEMENT DEVICE,Intervertebral fusion device with bone graft, lumbar,TRAY, SURGICAL, INSTRUMENT 1 NA
29 00889024320505 96-499-30001 96-499-30001 MAX,MQP,FSM Intervertebral fusion device with bone graft, lumbar,SPINAL VERTEBRAL BODY REPLA Intervertebral fusion device with bone graft, lumbar,SPINAL VERTEBRAL BODY REPLACEMENT DEVICE,TRAY, SURGICAL, INSTRUMENT 1 NA
30 00889024320499 96-499-20001 96-499-20001 MQP,MAX,FSM SPINAL VERTEBRAL BODY REPLACEMENT DEVICE,Intervertebral fusion device with bone SPINAL VERTEBRAL BODY REPLACEMENT DEVICE,Intervertebral fusion device with bone graft, lumbar,TRAY, SURGICAL, INSTRUMENT 1 NA
31 00889024320482 96-499-10001 96-499-10001 MQP,FSM,MAX SPINAL VERTEBRAL BODY REPLACEMENT DEVICE,TRAY, SURGICAL, INSTRUMENT,Intervertebr SPINAL VERTEBRAL BODY REPLACEMENT DEVICE,TRAY, SURGICAL, INSTRUMENT,Intervertebral fusion device with bone graft, lumbar 1 NA
32 00889024320031 96-215-21031 96-215-21031 GAD RETRACTOR 1 NA
33 00889024320024 96-215-21021 96-215-21021 GAD RETRACTOR 1 NA
34 00889024320017 96-215-21011 96-215-21011 GAD RETRACTOR 1 NA
35 00889024320000 96-215-21001 96-215-21001 GAD RETRACTOR 1 NA
36 00889024319998 96-215-20001 96-215-20001 GAD RETRACTOR 1 NA
37 00889024319981 96-215-19011 96-215-19011 GAD RETRACTOR 1 NA
38 00889024319974 96-215-19001 96-215-19001 GAD RETRACTOR 1 NA
39 00889024319967 96-215-18001 96-215-18001 GAD RETRACTOR 1 NA
40 00889024319950 96-215-17011 96-215-17011 GAD RETRACTOR 1 NA
41 00889024319943 96-215-17001 96-215-17001 GAD RETRACTOR 1 NA
42 00889024319936 96-215-16001 96-215-16001 GAD RETRACTOR 1 NA
43 00889024319929 96-215-15011 96-215-15011 GAD RETRACTOR 1 NA
44 00889024319912 96-215-15001 96-215-15001 GAD RETRACTOR 1 NA
45 00889024319905 96-215-14011 96-215-14011 GAD RETRACTOR 1 NA
46 00889024319899 96-215-14001 96-215-14001 GAD RETRACTOR 1 NA
47 00889024319882 96-215-13011 96-215-13011 GAD RETRACTOR 1 NA
48 00889024319875 96-215-13001 96-215-13001 GAD RETRACTOR 1 NA
49 00889024319868 96-215-12011 96-215-12011 GAD RETRACTOR 1 NA
50 00889024319851 96-215-12001 96-215-12001 GAD RETRACTOR 1 NA
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.
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.