MICRUS MICROCOIL SYSTEM, DELTAPAQ 10 CERECYTE, MODEL CDF

MICRUS MICROCOIL SYSTEM, DELTAPAQ 10 CERECYTE, MODEL CDF is an FDA 510(k)-cleared medical device (K080437) manufactured by Micrus Endovascular Corporation. This device is classified under the Neurology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on May 7, 2008. Regulation: 8.