SYNTHES HINDFOOT ARTHRODESIS NAIL SYSTEM— 510(k) K051678

Substantially Equivalent

Synthes (Usa)

FDA 510(k) clearance K051678 for SYNTHES HINDFOOT ARTHRODESIS NAIL SYSTEM, Substantially Equivalent on 2005-09-21. Applicant: Synthes (Usa).

Clearance details

Applicant: Synthes (Usa)
Product code: Code HSB
Advisory panel: Orthopedic
Date received: 2005-06-23
Decision date: 2005-09-21
Decision: Substantially Equivalent
Clearance type: Traditional
Location: West Chester, PA, US

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Adverse events under product code HSB

product code HSB

Death: 49
Injury: 12,083
Malfunction: 6,561
Other: 1
Total: 18,694

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.