UNITRAX V40 MODULAR ADAPTOR— 510(k) K954077

Name: FDA 510(k) clearance K954077
Creator: U.S. Food and Drug Administration
Published: 1995-11-15

Substantially Equivalent

Howmedica Corp.

FDA 510(k) clearance K954077 for UNITRAX V40 MODULAR ADAPTOR, Substantially Equivalent on 1995-11-15. 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: 1995-08-30
Decision date: 1995-11-15
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 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.