MODIFICATION TO SYNTHES CERVIFIX SYSTEM— 510(k) K030377

Substantially Equivalent

Synthes (Usa)

FDA 510(k) clearance K030377 for MODIFICATION TO SYNTHES CERVIFIX SYSTEM, Substantially Equivalent on 2003-03-06. Applicant: Synthes (Usa).

Clearance details

Applicant: Synthes (Usa)
Product code: Code MNI
Advisory panel: Orthopedic
Date received: 2003-02-05
Decision date: 2003-03-06
Decision: Substantially Equivalent
Clearance type: Special
Location: Paoli, PA, US

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Adverse events under product code MNI

product code MNI

Injury: 641
Total: 641

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.