SYNTHES (USA) MIDFACIAL SYSTEM— 510(k) K953806

Substantially Equivalent

Synthes (Usa)

FDA 510(k) clearance K953806 for SYNTHES (USA) MIDFACIAL SYSTEM, Substantially Equivalent on 1996-03-08. Applicant: Synthes (Usa).

Clearance details

Applicant: Synthes (Usa)
Product code: Code JEY
Advisory panel: Dental
Date received: 1995-08-10
Decision date: 1996-03-08
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Paoli, PA, US

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Adverse events under product code JEY

product code JEY

Injury: 1,542
Malfunction: 2,292
Total: 3,834

Source: openFDA MAUDE database, 2020-01-01 through 2026-04-23. Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

Data sourced from openFDA. This site is unofficial and independent of the FDA.