
Artiberia
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9-190,9-200,9-210,9-220 AMPUTATION KNIVES, VARIOUS is an FDA 510(k)-cleared medical device (K851752) manufactured by Artiberia. This device is classified under the General, Plastic Surgery specialty. FDA Device Class I (General Controls) — lowest risk category. FDA clearance granted on June 19, 1985. Regulation: 8.