COVER, BURR HOLE
FDA product code GXR · Class 2 · 24 devices · 264 reports · 1 deaths reported · 0 devices named in recalls
- GUARDIAN™ 6010St. Jude Medical, Inc. · COVER, BURR HOLE151 reports
- GUARDIAN™ 6010St. Jude Medical, Inc. · COVER, BURR HOLE1 death25 reports
- "1.5MM" SYSTEM 95-1505Biomet Microfixation, Inc · COVER, BURR HOLE23 reports
- "1.5MM" SYSTEM 91-6105Biomet Microfixation, Inc · COVER, BURR HOLE20 reports
- CRANIOFIX® ABSORBABLE FF016Aesculap AG · COVER, BURR HOLE8 reports
- "1.5MM" SYSTEM 91-6106Biomet Microfixation, Inc · COVER, BURR HOLE7 reports
- 1.5MM SYSTEM 91-6105X-50Biomet Microfixation, Inc · COVER, BURR HOLE6 reports
- TMS SYSTEM 25-2007Biomet Microfixation, Inc · COVER, BURR HOLE3 reports
- 1.5MM SYSTEM 01-7114Biomet Microfixation, Inc · COVER, BURR HOLE2 reports
- "1.5MM" SYSTEM 95-6107Biomet Microfixation, Inc · COVER, BURR HOLE2 reports
- Burr Hole Cover 8110Neuropace, Inc. · COVER, BURR HOLE2 reports
- CRANIOFIX® ABSORBABLE FF017Aesculap AG · COVER, BURR HOLE2 reports
- NA 446.611Synthes GmbH · COVER, BURR HOLE2 reports
- NA 3550S-01Medtronic, Inc. · COVER, BURR HOLE1 report
- 1.5MM SYSTEM 01-7309Biomet Microfixation, Inc · COVER, BURR HOLE1 report
- 1.5MM SYSTEM 01-7347Biomet Microfixation, Inc · COVER, BURR HOLE1 report
- "2.0MM" SYSTEM PLATE 01-9207Biomet Microfixation, Inc · COVER, BURR HOLE1 report
- "2.0MM" SYSTEM PLATE 01-9262Biomet Microfixation, Inc · COVER, BURR HOLE1 report
- "2.0MM" SYSTEM 95-6205Biomet Microfixation, Inc · COVER, BURR HOLE1 report
- THINFLAP SYSTEM 91-6904Biomet Microfixation, Inc · COVER, BURR HOLE1 report
- 1.5MM SYSTEM - CRANIOCURVE (TM) MESH 01-9522Biomet Microfixation, Inc · COVER, BURR HOLE1 report
- GUARDIAN™ 6015St. Jude Medical, Inc. · COVER, BURR HOLE1 report
- RapidSorb 851.801.01SSynthes GmbH · COVER, BURR HOLE1 report
- NA SR-6000Medtronic, Inc. · COVER, BURR HOLE1 report