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RIVA Posterior Fixation System
XENIX MEDICAL LLC · Model FG1-51-125030 · UDI-DI 00840493410296
1
510(k) clearances
0
Adverse events
1
Recalls
2
Facilities
Description
BONE SCREW, CANNULATED, FENESTRATED, 12.5mm X 30mm
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2003-04-04 | Ventana Medical Systems Inc | Increased level of non-specific or background staining. |
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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.