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Synthes GmbH · Model 495.423 · UDI-DI 10705034785752
10
510(k) clearances
198
Adverse events (5 deaths)
0
Recalls
26
Facilities
Description
END RING 17MM X 22MM ANTEROLATERAL/5 DEG CONVEX(TI)
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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.