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Synthes GmbH · Model 236.430S · UDI-DI 10886982160645

KTW Prescription
1
510(k) clearances
916
Adverse events
57
Recalls
51
Facilities

Description

115 DEG BIFURCATED PLATE 35MM/5MM - STERILE

Recalls

DateFirmReason
2010-10-27Synthes USA (HQ), Inc.Potential for out of specification star grind teeth.
2010-10-27Synthes USA (HQ), Inc.Potential for out of specification star grind teeth.
2010-10-27Synthes USA (HQ), Inc.Potential for out of specification star grind teeth.
2010-10-27Synthes USA (HQ), Inc.Potential for out of specification star grind teeth.
2010-10-27Synthes USA (HQ), Inc.Potential for out of specification star grind teeth.
2010-10-27Synthes USA (HQ), Inc.Potential for out of specification star grind teeth.
2010-10-27Synthes USA (HQ), Inc.Potential for out of specification star grind teeth.
2010-10-27Synthes USA (HQ), Inc.Potential for out of specification star grind teeth.
2010-10-27Synthes USA (HQ), Inc.Potential for out of specification star grind teeth.
2010-10-27Synthes USA (HQ), Inc.Potential for out of specification star grind teeth.

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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.