TFNA FENESTRATED SCREW 110MM - STERILE Adverse Event — Injury (MDR 8030965-2020-03118)
TFNA FENESTRATED SCREW 110MM - STERILE Adverse Event — Injury (MDR 8030965-2020-03118) is one of 9,000 device adverse events in the DeviceEvents dataset. Key details — Device: TFNA FENESTRATED SCREW 110MM - STERILE; Generic name: ROD,FIXATION,INTRAMEDULLARY; Manufacturer: OBERDORF SYNTHES PRODUKTIONS GMBH.
| Device | TFNA FENESTRATED SCREW 110MM - STERILE |
|---|---|
| Generic name | ROD,FIXATION,INTRAMEDULLARY |
| Manufacturer | OBERDORF SYNTHES PRODUKTIONS GMBH |
| Report number | 8030965-2020-03118 |
| Event type | Injury |
| Product problem | Y |
| Date received | 2020-04-27 |
| Report source | COMPANY REPRESENTATIVE, FOREIG |
| Narrative | ONLY EVENT YEAR IS KNOWN: 2020. ADDITIONAL DEVICE PRODUCT CODES: KTT. COMPLAINANT PART IS NOT EXPECTED TO BE RETURNED FOR MANUFACTURER REVIEW/INVESTIGATION. PART NUMBER: 04.038.210S. LOT NUMBER: H831245. PART MANUFACTURING DATE: FEBRUARY 21, 2019. MANUFACTURING SITE: (B)(4). PART EXPIRATION DATE: FEBRUARY 1, 2029. NONCONFORMANCE NOTED: N/A. A REVIEW OF THE DEVICE HISTORY RECORD REVEALED NO COMPLAI |
| Source | openFDA MAUDE (device adverse events) |
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