TRIATHLON PS FEM COMPONENT, CEMENTED Adverse Event — Injury (MDR 2249697-2008-00039)
TRIATHLON PS FEM COMPONENT, CEMENTED Adverse Event — Injury (MDR 2249697-2008-00039) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: TRIATHLON PS FEM COMPONENT, CEMENTED; Generic name: IMPLANT; Manufacturer: STRYKER ORTHOPAEDICS MAHWAH.
| Device | TRIATHLON PS FEM COMPONENT, CEMENTED |
|---|---|
| Generic name | IMPLANT |
| Manufacturer | STRYKER ORTHOPAEDICS MAHWAH |
| Report number | 2249697-2008-00039 |
| Event type | Injury |
| Product problem | N |
| Date received | 2008-02-19 |
| Report source | Company representation |
| Narrative | IT WAS REPORTED THAT, "PATIENT PRESENTED WITH FLUID IN THE KNEE SEVERAL MONTHS AFTER TRIATHLON TKR. KNEE WAS DRAINED. NO SIGN OF INFECTION." |
| Source | openFDA MAUDE (device adverse events) |
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