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SYNTHES (U.S.A.) LP · Model SD399.851 · UDI-DI 10886982007117

HWM Prescription

510(k) clearances

749

Adverse events

Recalls

254

Facilities

Description

OSTEOTOME/90 DEGREE BEND 500MM

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Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.

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Data 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.