TRIDENT HEMISPHERICAL SOLID BACK SHELL Adverse Event — Injury (MDR 9616680-2008-00032)
TRIDENT HEMISPHERICAL SOLID BACK SHELL Adverse Event — Injury (MDR 9616680-2008-00032) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: TRIDENT HEMISPHERICAL SOLID BACK SHELL; Generic name: IMPLANT; Manufacturer: STRYKER ORTHOPAEDICS, CORK.
| Device | TRIDENT HEMISPHERICAL SOLID BACK SHELL |
|---|---|
| Generic name | IMPLANT |
| Manufacturer | STRYKER ORTHOPAEDICS, CORK |
| Report number | 9616680-2008-00032 |
| Event type | Injury |
| Product problem | N |
| Date received | 2008-02-19 |
| Report source | Company representation |
| Narrative | IT WAS REPORTED THAT "TRIDENT HEMI SHELL SPUN INTO A VERTICAL POSITION." |
| Source | openFDA MAUDE (device adverse events) |
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