ANKLE-FOOT CAST/SPLINT— 510(k) K811690

Name: FDA 510(k) clearance K811690
Creator: U.S. Food and Drug Administration
Published: 1981-06-25

Substantially Equivalent

Surgical Appliance Industries, Inc.

FDA 510(k) clearance K811690 for ANKLE-FOOT CAST/SPLINT, Substantially Equivalent on 1981-06-25. Applicant: Surgical Appliance Industries, Inc.. Device class: 1.

Clearance details

Applicant: Surgical Appliance Industries, Inc.
Product code: Code IQI
Device class: Class 1
Regulation: 21 CFR 890.3475
Advisory panel: Physical Medicine
Date received: 1981-06-15
Decision date: 1981-06-25
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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