
Smith & Nephew Endoscopy, Inc.
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SURGICAL KIT-ACUFEX MOSAICPLASTY SYSTEM is an FDA 510(k)-cleared medical device (K962789) manufactured by Smith & Nephew Endoscopy, Inc.. This device is classified under the General, Plastic Surgery specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on August 13, 1996. Regulation: 8.