HOWMEDICCA MODULAR PROXIMAL HUMERUS REPLACEMENT SYSTEM— 510(k) K954559

Name: FDA 510(k) clearance K954559
Creator: U.S. Food and Drug Administration
Published: 1996-07-12

Substantially Equivalent

Howmedica Corp.

FDA 510(k) clearance K954559 for HOWMEDICCA MODULAR PROXIMAL HUMERUS REPLACEMENT SYSTEM, Substantially Equivalent on 1996-07-12. Applicant: Howmedica Corp.. Device class: 2.

Clearance details

Applicant: Howmedica Corp.
Product code: Code HSD
Device class: Class 2
Regulation: 21 CFR 888.3690
Advisory panel: Orthopedic
Date received: 1995-10-02
Decision date: 1996-07-12
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Rutherford, NJ, US

Download summary PDF View on FDA.gov ↗

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Adverse events under product code HSD

product code HSD

Injury: 3,425
Malfunction: 531
Total: 3,956

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.