LIMB ORHTOSIS— 510(k) K810222

Name: FDA 510(k) clearance K810222
Creator: U.S. Food and Drug Administration
Published: 1981-02-04

Substantially Equivalent

Medical Design & Manufacturing Corp.

FDA 510(k) clearance K810222 for LIMB ORHTOSIS, Substantially Equivalent on 1981-02-04. Applicant: Medical Design & Manufacturing Corp.. Device class: 1.

Clearance details

Applicant: Medical Design & Manufacturing Corp.
Product code: Code ITQ
Device class: Class 1
Regulation: 21 CFR 890.3475
Advisory panel: Physical Medicine
Date received: 1981-01-27
Decision date: 1981-02-04
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Walker, MI, US

Download summary PDF View on FDA.gov ↗

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