BARRICADE EMBOLIZATION COIL SYSTEM

BARRICADE EMBOLIZATION COIL SYSTEM is an FDA 510(k)-cleared medical device (K123338) manufactured by Blockade Medical. This device is classified under the Neurology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on March 27, 2013. Regulation: 8.