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Synthes GmbH · Model 03.501.443 · UDI-DI 10887587077574
1
510(k) clearances
39,163
Adverse events (74 deaths)
0
Recalls
517
Facilities
Description
MATRIXSTERNUM HANDLE FOR SCREW GUIDE
Query this across every FDA database — by API.
Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.
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.