
Bowen & Company, Inc.
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MORGAN ARTHROSCOPIC MENESUS & SYNOVIAL RASP is an FDA 510(k)-cleared medical device (K853601) manufactured by Bowen & Company, Inc.. This device is classified under the General, Plastic Surgery specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on September 15, 1985. Regulation: 8.