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RIVA Posterior Fixation System
XENIX MEDICAL LLC · Model FG1-52-115065 · UDI-DI 00840493411774
1
510(k) clearances
4
Adverse events (1 deaths)
1
Recalls
4
Facilities
Description
BONE SCREW, CANNULATED, CORTICAL CANCELLOUS, 11.5mm X 65mm
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2021-05-04 | Medtronic Vascular | The component part numbers intended for shipment to a third-party, where they are further processed into kits and sterilized were instead shipped directly to customers. |
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Get your free API keyRead the docsData compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.