ARTHREX FINGERSHIELD FINGER GUARD, MODEL AR-7199-XX— 510(k) K052387

Name: FDA 510(k) clearance K052387
Creator: U.S. Food and Drug Administration
Published: 2005-11-29

Substantially Equivalent

Arthrex, Inc.

FDA 510(k) clearance K052387 for ARTHREX FINGERSHIELD FINGER GUARD, MODEL AR-7199-XX, Substantially Equivalent on 2005-11-29. Applicant: Arthrex, Inc.. Device class: 1.

Clearance details

Applicant: Arthrex, Inc.
Product code: Code LZB
Device class: Class 1
Regulation: 21 CFR 880.6250
Advisory panel: General Hospital
Date received: 2005-08-31
Decision date: 2005-11-29
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Naples, FL, US

Download summary PDF View on FDA.gov ↗

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