
United States Surgical, A Division of Tyco Healthc
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SURGICAL INSTRUMENT GUIDE is an FDA 510(k)-cleared medical device (K950007) manufactured by United States Surgical, A Division of Tyco Healthc. This device is classified under the General, Plastic Surgery specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on March 14, 1995. Regulation: 8.