
Terumo Cardiovascular Systems Corporation
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VIRTUOSAPH PLUS ENDOSCOPIC VESSEL HARVESTING SYSTEM is an FDA 510(k)-cleared medical device (K140008) manufactured by Terumo Cardiovascular Systems Corporation. This device is classified under the General, Plastic Surgery specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on October 30, 2014. Regulation: 8.