KNEE AID— 510(k) K760002

Substantially Equivalent

Zimmer, Inc.

FDA 510(k) clearance K760002 for KNEE AID, Substantially Equivalent on 1976-07-26. Applicant: Zimmer, Inc.. Device class: 1.

Clearance details

Applicant: Zimmer, Inc.
Product code: Product code IQI
Device class: Class 1
Regulation: 21 CFR 890.3475
Advisory panel: Physical Medicine
Date received: 1976-05-26
Decision date: 1976-07-26
Decision: Substantially Equivalent
Clearance type: Traditional
Location: 1831 Olive St. St. Louis, MO, 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.