| Primary Device ID | 00643169774582 |
| NIH Device Record Key | d5e72381-3d17-4afd-a19c-39ad109b43b6 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | MTS Knee |
| Version Model Number | 90-SRK-210106 |
| Company DUNS | 030200852 |
| Company Name | MEDTRONIC, INC. |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | false |
| MRI Safety Status | Labeling does not contain MRI Safety Information |
| Human Cell/Tissue Product | false |
| Device Kit | false |
| Device Combination Product | false |
| Single Use | false |
| Lot Batch | true |
| Serial Number | false |
| Manufacturing Date | false |
| Expiration Date | false |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | true |
| OTC Over-The-Counter | false |
| Phone | +1(800)633-8766 |
| Corporate.UDI@medtronic.com | |
| Phone | +1(800)633-8766 |
| Corporate.UDI@medtronic.com | |
| Phone | +1(800)633-8766 |
| Corporate.UDI@medtronic.com | |
| Phone | +1(800)633-8766 |
| Corporate.UDI@medtronic.com | |
| Phone | +1(800)633-8766 |
| Corporate.UDI@medtronic.com | |
| Phone | +1(800)633-8766 |
| Corporate.UDI@medtronic.com | |
| Phone | +1(800)633-8766 |
| Corporate.UDI@medtronic.com | |
| Phone | +1(800)633-8766 |
| Corporate.UDI@medtronic.com | |
| Phone | +1(800)633-8766 |
| Corporate.UDI@medtronic.com | |
| Phone | +1(800)633-8766 |
| Corporate.UDI@medtronic.com | |
| Phone | +1(800)633-8766 |
| Corporate.UDI@medtronic.com | |
| Phone | +1(800)633-8766 |
| Corporate.UDI@medtronic.com | |
| Phone | +1(800)633-8766 |
| Corporate.UDI@medtronic.com | |
| Phone | +1(800)633-8766 |
| Corporate.UDI@medtronic.com | |
| Phone | +1(800)633-8766 |
| Corporate.UDI@medtronic.com |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00643169774582 [Primary] |
| JWH | PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER |
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[00643169774582]
Moist Heat or Steam Sterilization
[00643169774582]
Moist Heat or Steam Sterilization
[00643169774582]
Moist Heat or Steam Sterilization
[00643169774582]
Moist Heat or Steam Sterilization
[00643169774582]
Moist Heat or Steam Sterilization
[00643169774582]
Moist Heat or Steam Sterilization
[00643169774582]
Moist Heat or Steam Sterilization
[00643169774582]
Moist Heat or Steam Sterilization
[00643169774582]
Moist Heat or Steam Sterilization
[00643169774582]
Moist Heat or Steam Sterilization
[00643169774582]
Moist Heat or Steam Sterilization
[00643169774582]
Moist Heat or Steam Sterilization
[00643169774582]
Moist Heat or Steam Sterilization
[00643169774582]
Moist Heat or Steam Sterilization
[00643169774582]
Moist Heat or Steam Sterilization
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 2 |
| Public Version Date | 2019-02-07 |
| Device Publish Date | 2018-12-30 |
| 00643169778337 | TRAY 90-SRK-800033 FEMORAL TRIALS PS |
| 00643169778320 | TRAY 90-SRK-800013 POLY TRIALS PS |
| 00643169778313 | TRAY 90-SRK-800015 POLY TRIALS MPCS R |
| 00643169778306 | TRAY 90-SRK-800014 POLY TRIALS MPCS L |
| 00643169778290 | TRAY 90-SRK-800012 POLY TRIALS UCCS |
| 00643169778283 | TRAY 90-SRK-800040 PATELLA PREP |
| 00643169778276 | TRAY 90-SRK-800031 FEMORAL TRIAL CR/CS |
| 00643169778245 | TRAY 90-SRK-800030 FEMORAL PREP |
| 00643169778221 | TRAY 90-SRK-800020 TIBIAL PREP |
| 00643169778214 | TRAY 90-SRK-800011 POLY TRIALS CR/CS |
| 00643169774582 | TRIAL 90-SRK-210106 TIBIAL TRAY SIZE 6 |
| 00643169774575 | TRIAL 90-SRK-210105 TIBIAL TRAY SIZE 5 |
| 00643169774568 | TRIAL 90-SRK-210104 TIBIAL TRAY SIZE 4 |
| 00643169774551 | TRIAL 90-SRK-210103 TIBIAL TRAY SIZE 3 |
| 00643169774544 | TRIAL 90-SRK-210102 TIBIAL TRAY SIZE 2 |
| 00643169774537 | TRIAL 90-SRK-210101 TIBIAL TRAY SIZE 1 |
| 00643169774315 | TOOL 90-SRK-100010 POLY REMOVAL |
| 00643169774308 | IMPACTOR 90-SRK-100000 POLY |
| 00643169774292 | EXTRACTOR 90-SRK-201310 TIBIAL TRAY |
| 00643169774285 | IMPACTOR 90-SRK-201300 TIBIAL TRAY |
| 00643169774278 | PUNCH 90-SRK-201222 KEEL 3-6 |
| 00643169774261 | PUNCH 90-SRK-201221 KEEL 1-2 |
| 00643169774223 | CUTTING BLOCK 90-SRK-201011 TIBIAL RIGHT |
| 00643169774216 | CUTTING BLOCK 90-SRK-201012 TIBIAL LEFT |
| 00643169774193 | STYLUS 90-SRK-201101 TIBIAL RESECT-10MM |
| 00643169774179 | CLAMP 90-SRK-201002 TIBIAL ANKLE |
| 00643169774162 | GUIDE 90-SRK-201000 TIBIAL ALIGNMENT |
| 00643169774155 | IMPACTOR 90-SRK-300420 FEMORAL NOTCH |
| 00643169774148 | IMPACTOR 90-SRK-300410 FEMORAL CONDYLE |
| 00643169774124 | WING 90-SRK-300210 ANGEL |
| 00643169774117 | CUTTING BLOCK 90-SRK-300206 4 IN 1 SZ 6 |
| 00643169774100 | CUTTING BLOCK 90-SRK-300205 4 IN 1 SZ 5 |
| 00643169774094 | CUTTING BLOCK 90-SRK-300204 4 IN 1 SZ 4 |
| 00643169774087 | CUTTING BLOCK 90-SRK-300203 4 IN 1 SZ 3 |
| 00643169774070 | CUTTING BLOCK 90-SRK-300202 4 IN 1 SZ 2 |
| 00643169774063 | CUTTING BLOCK 90-SRK-300201 4 IN 1 SZ 1 |
| 00643169774049 | CUTTING BLOCK 90-SRK-300023 DF 3 DEG |
| 00643169774032 | CUTTING BLOCK 90-SRK-300020 DF 0 DEG |
| 00643169774025 | GUIDE 90-SRK-300012 DF RESECTION |
| 00643169774018 | GUIDE 90-SRK-300011 DF ANGLE |
| 00643169774001 | ROD 90-SRK-300002 IM |
| 00643169771741 | TOOL 90-SRK-100050 POLY TRIAL REMOVAL |
| 00643169771734 | GUIDE 90-SRK-300220 4 IN 1 AP ADJUSTMENT |
| 00643169771727 | PUCK 90-SRK-460024 PATELLA - ROUND 36 |
| 00643169771710 | PUCK 90-SRK-460023 PATELLA - ROUND 33 |
| 00643169771703 | PUCK 90-SRK-460022 PATELLA - ROUND 31 |
| 00643169771697 | PUCK 90-SRK-460021 PATELLA - ROUND 29 |
| 00643169771680 | PUCK 90-SRK-460014 PATELLA - OVAL 41 |
| 00643169771673 | PUCK 90-SRK-460013 PATELLA - OVAL 38 |
| 00643169771666 | PUCK 90-SRK-460012 PATELLA - OVAL 35 |