TRI TS BASEPLATE SIZE 1 Adverse Event — Injury (MDR 0002249697-2020-00805)
TRI TS BASEPLATE SIZE 1 Adverse Event — Injury (MDR 0002249697-2020-00805) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: TRI TS BASEPLATE SIZE 1; Generic name: PROSTHESIS, KNEE, PATELLO/FEMOROTIBIAL, SEMI-CONSTRAINED, UN; Manufacturer: STRYKER ORTHOPAEDICS-MAHWAH.
| Device | TRI TS BASEPLATE SIZE 1 |
|---|---|
| Generic name | PROSTHESIS, KNEE, PATELLO/FEMOROTIBIAL, SEMI-CONSTRAINED, UN |
| Manufacturer | STRYKER ORTHOPAEDICS-MAHWAH |
| Report number | 0002249697-2020-00805 |
| Event type | Injury |
| Product problem | N |
| Date received | 2020-04-27 |
| 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) |
🔍 Search all device adverse events →
$1999/mo
Try DeviceEvents →