C.C.F. FEMORAL DEBRIDEMENT PROBE— 510(k) K790996

Substantially Equivalent

Depuy, Inc.

FDA 510(k) clearance K790996 for C.C.F. FEMORAL DEBRIDEMENT PROBE, Substantially Equivalent on 1979-06-27. Applicant: Depuy, Inc..

Clearance details

Applicant: Depuy, Inc.
Product code: Code HTO
Advisory panel: Orthopedic
Date received: 1979-05-29
Decision date: 1979-06-27
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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Adverse events under product code HTO

product code HTO

Injury: 404
Malfunction: 20,305
Total: 20,709

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.