MODIFIED TOWNLEY UNICONDYLAR KNEE— 510(k) K871118

Name: FDA 510(k) clearance K871118
Creator: U.S. Food and Drug Administration
Published: 1987-04-06

Substantially Equivalent for Some Indications

Depuy, Inc.

FDA 510(k) clearance K871118 for MODIFIED TOWNLEY UNICONDYLAR KNEE, Substantially Equivalent for Some Indications on 1987-04-06. Applicant: Depuy, Inc.. Device class: 2.

Clearance details

Applicant: Depuy, Inc.
Product code: Code KYK
Device class: Class 2
Regulation: 21 CFR 888.3500
Advisory panel: Orthopedic
Date received: 1987-03-19
Decision date: 1987-04-06
Decision: Substantially Equivalent for Some Indications
Clearance type: Traditional
Location: Warsaw, IN, US

Download summary PDF View on FDA.gov ↗

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