INTERLOCK-35 FIBERED IDC OCCLUSION SYSTEM

INTERLOCK-35 FIBERED IDC OCCLUSION SYSTEM is an FDA 510(k)-cleared medical device (K110295) manufactured by Boston Scientific Corp. This device is classified under the Cardiovascular specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on March 2, 2011. Regulation: 8.