CONSENSUS 26MM COCRMO FEMORAL HEAD— 510(k) K960151

Substantially Equivalent

U.S. Medical Products, Inc.

FDA 510(k) clearance K960151 for CONSENSUS 26MM COCRMO FEMORAL HEAD, Substantially Equivalent on 1996-02-21. Applicant: U.S. Medical Products, Inc..

Clearance details

Applicant: U.S. Medical Products, Inc.
Product code: Code JDI
Advisory panel: Orthopedic
Date received: 1996-01-11
Decision date: 1996-02-21
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Austin, TX, US

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Adverse events under product code JDI

product code JDI

Death: 65
Injury: 12,943
Malfunction: 1,681
Total: 14,689

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.