ILLIZAROV Adverse Event — Injury (MDR 1020279-2008-00053)
ILLIZAROV Adverse Event — Injury (MDR 1020279-2008-00053) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: ILLIZAROV; Generic name: EXTERNAL FIXATION; Manufacturer: SMITH & NEPHEW, INC., ORTHOPAEDIC DIV..
| Device | ILLIZAROV |
|---|---|
| Generic name | EXTERNAL FIXATION |
| Manufacturer | SMITH & NEPHEW, INC., ORTHOPAEDIC DIV. |
| Report number | 1020279-2008-00053 |
| Event type | Injury |
| Product problem | N |
| Date received | 2008-02-19 |
| Report source | Company representation |
| Narrative | BECAUSE IT WAS REPORTED BY THE PT'S SURGEON THAT INTERVENTION WAS REQUIRED AS A RESULT OF USAGE OF THE DEVICE AND/OR EXTERNAL FACTORS OR CIRCUMSTANCES WERE IDENTIFIED THAT MAY HAVE CONTRIBUTED TO THE ADVERSE EVENT. |
| Source | openFDA MAUDE (device adverse events) |
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