Bit, Drill
Medtronic Sofamor Danek Usa, Inc.'s record for this product code
MDR events23All time
Recalls0All time
510(k) clearances0All time
Recent MDR events
23 adverse event reports on file
- UCSSNov 24, 2023Malfunction1030489-2023-00800
- SPECIALS-CERVICALMay 3, 2023Injury1030489-2023-00326
- UCSSJun 17, 2022Malfunction1030489-2022-00548
- UCSSNov 26, 2021Malfunction1030489-2021-01461
- UCSSAug 18, 2021Malfunction1030489-2021-01057
- MEDTRONIC DRILL BITMay 5, 2021MalfunctionMW5101195
- UCSSFeb 15, 2021Malfunction1030489-2021-00195
- UCSSJan 11, 2021Malfunction1030489-2021-00038
- UCSSDec 16, 2020Injury1030489-2020-01805
- INFINITYJul 17, 2020Injury1030489-2020-00929
Recalls
0 recall events for this product code
No recalls on file for Medtronic Sofamor Danek Usa, Inc. under this product code.
510(k) clearances
0 clearances for this product code
No 510(k) clearances on file for Medtronic Sofamor Danek Usa, Inc. under this product code.