UNKNOWN_SCORPIO FEMORAL COMPONENT Adverse Event — Injury (MDR 0002249697-2020-00824)
UNKNOWN_SCORPIO FEMORAL COMPONENT Adverse Event — Injury (MDR 0002249697-2020-00824) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: UNKNOWN_SCORPIO FEMORAL COMPONENT; Generic name: PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEM; Manufacturer: STRYKER ORTHOPAEDICS-
| Device | UNKNOWN_SCORPIO FEMORAL COMPONENT |
|---|---|
| Generic name | PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEM |
| Manufacturer | STRYKER ORTHOPAEDICS-MAHWAH |
| Report number | 0002249697-2020-00824 |
| Event type | Injury |
| Product problem | N |
| Date received | 2020-04-28 |
| Report source | HEALTH PROFESSIONAL, OTHER |
| Narrative | IT WAS NOTED THAT THE DEVICE IS NOT AVAILABLE FOR EVALUATION. SHOULD ADDITIONAL INFORMATION BECOME AVAILABLE, IT WILL BE PROVIDED IN A SUPPLEMENTAL REPORT UPON COMPLETION OF THE INVESTIGATION. |
| Source | openFDA MAUDE (device adverse events) |
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