POROCOAT (R) PROXIMAL FEMORAL THIRD PROSTHESIS— 510(k) K872025

Substantially Equivalent for Some Indications

Depuy, Inc.

FDA 510(k) clearance K872025 for POROCOAT (R) PROXIMAL FEMORAL THIRD PROSTHESIS, Substantially Equivalent for Some Indications on 1987-08-18. Applicant: Depuy, Inc..

Clearance details

Applicant: Depuy, Inc.
Product code: Code KWL
Advisory panel: Orthopedic
Date received: 1987-05-26
Decision date: 1987-08-18
Decision: Substantially Equivalent for Some Indications
Clearance type: Traditional
Location: Warsaw, IN, US

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Adverse events under product code KWL

product code KWL

Injury: 523
Total: 523

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.