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

Name: FDA 510(k) clearance K896853
Creator: U.S. Food and Drug Administration
Published: 1990-05-02

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.. Device class: 2.

Clearance details

Applicant: Howmedica Corp.
Product code: Code KWL
Device class: Class 2
Regulation: 21 CFR 888.3360
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 ↗

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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.