WMT MODULAR ULNAR HEAD IMPLANT— 510(k) K020274

Name: FDA 510(k) clearance K020274
Creator: U.S. Food and Drug Administration
Published: 2002-02-22

Substantially Equivalent

Wrightmedicaltechnologyinc

FDA 510(k) clearance K020274 for WMT MODULAR ULNAR HEAD IMPLANT, Substantially Equivalent on 2002-02-22. Applicant: Wrightmedicaltechnologyinc. Device class: 2.

Clearance details

Applicant: Wrightmedicaltechnologyinc
Product code: Code KXE
Device class: Class 2
Regulation: 21 CFR 888.3810
Advisory panel: Orthopedic
Date received: 2002-01-28
Decision date: 2002-02-22
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Arlington, TN, US

Download summary PDF View on FDA.gov ↗

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Data sourced from openFDA. This site is unofficial and independent of the FDA.