
Arthrex, Inc.
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ARTHREX FINGERSHIELD FINGER GUARD, MODEL AR-7199-XX is an FDA 510(k)-cleared medical device (K052387) manufactured by Arthrex, Inc.. This device is classified under the General Hospital specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on November 28, 2005. Regulation: 8.

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