HOWMEDICA PRECISION OSTEOLOCK FEMORAL COMPONENT— 510(k) K881983

Substantially Equivalent

Howmedica Corp.

FDA 510(k) clearance K881983 for HOWMEDICA PRECISION OSTEOLOCK FEMORAL COMPONENT, Substantially Equivalent on 1988-10-06. Applicant: Howmedica Corp..

Clearance details

Applicant: Howmedica Corp.
Product code: Code LWJ
Advisory panel: Orthopedic
Date received: 1988-05-12
Decision date: 1988-10-06
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Rutherford, NJ, US

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Adverse events under product code LWJ

product code LWJ

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.