PRECISION OSTEOLOCK FEMORAL COMP. TITANIUM PLASMA— 510(k) K896853

Substantially Equivalent for Some Indications

Howmedica Corp.

FDA 510(k) clearance K896853 for PRECISION OSTEOLOCK FEMORAL COMP. TITANIUM PLASMA, Substantially Equivalent for Some Indications on 1990-05-02. Applicant: Howmedica Corp..

Clearance details

Applicant: Howmedica Corp.
Product code: Code KWL
Advisory panel: Orthopedic
Date received: 1989-12-05
Decision date: 1990-05-02
Decision: Substantially Equivalent for Some Indications
Clearance type: Traditional
Location: Rutherford, NJ, US

Download summary PDF View on FDA.gov ↗

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.