MICRUS MODIFIED MICROCOIL SYSTEM, CERECYTE

MICRUS MODIFIED MICROCOIL SYSTEM, CERECYTE is an FDA 510(k)-cleared medical device (K033813) manufactured by Micrus Corp.. This device is classified under the Neurology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on February 3, 2004. Regulation: 8.