MODIFICATION TO VNUS CLOSURE SYSTEM

MODIFICATION TO VNUS CLOSURE SYSTEM is an FDA 510(k)-cleared medical device (K030557) manufactured by Vnus Medical Technologies, Inc.. 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 March 10, 2003. Regulation: 8.