BRÅNEMARK SYSTEM MK III GROOVY RP 4X10MM Adverse Event — Injury (MDR 9611993-2020-21604)
BRÅNEMARK SYSTEM MK III GROOVY RP 4X10MM Adverse Event — Injury (MDR 9611993-2020-21604) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: BRÅNEMARK SYSTEM MK III GROOVY RP 4X10MM; Generic name: ENDOSSEOUS DENTAL IMPLANT; Manufacturer: NOBEL BIOCARE AB.
| Device | BRÅNEMARK SYSTEM MK III GROOVY RP 4X10MM |
|---|---|
| Generic name | ENDOSSEOUS DENTAL IMPLANT |
| Manufacturer | NOBEL BIOCARE AB |
| Report number | 9611993-2020-21604 |
| Event type | Injury |
| Product problem | N |
| Date received | 2020-04-28 |
| Report source | HEALTH PROFESSIONAL |
| Narrative | IMPLANT FAILED DUE TO LOSS OF OSSEOINTEGRATION. |
| Source | openFDA MAUDE (device adverse events) |
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