SYNTHES PROXIMAL FEMORAL NAIL(PFN) SYSTEM MODIFICATION— 510(k) K973240

Substantially Equivalent

Synthes (Usa)

FDA 510(k) clearance K973240 for SYNTHES PROXIMAL FEMORAL NAIL(PFN) SYSTEM MODIFICATION, Substantially Equivalent on 1997-11-20. Applicant: Synthes (Usa).

Clearance details

Applicant: Synthes (Usa)
Product code: Code HTY
Advisory panel: Orthopedic
Date received: 1997-08-28
Decision date: 1997-11-20
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Paoli, PA, US

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Adverse events under product code HTY

product code HTY

Injury: 544
Total: 544

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.