TRIDENT HEMISPHERICAL CLUSTER HOLE SHELL Adverse Event — Injury (MDR 9616680-2008-00034)
TRIDENT HEMISPHERICAL CLUSTER HOLE SHELL Adverse Event — Injury (MDR 9616680-2008-00034) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: TRIDENT HEMISPHERICAL CLUSTER HOLE SHELL; Generic name: IMPLANT; Manufacturer: STRYKER ORTHOPAEDICS CORK.
| Device | TRIDENT HEMISPHERICAL CLUSTER HOLE SHELL |
|---|---|
| Generic name | IMPLANT |
| Manufacturer | STRYKER ORTHOPAEDICS CORK |
| Report number | 9616680-2008-00034 |
| Event type | Injury |
| Product problem | N |
| Date received | 2008-02-19 |
| Report source | Company representation |
| Narrative | IT WAS REPORTED THAT THE PATIENT WAS REVISED DUE TO MALALIGNMENT. TRITANIUM HEMI CUP WAS IMPLANTED IN PLACE OF TRIDENT HEMI CUP. |
| Source | openFDA MAUDE (device adverse events) |
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