MICRUS MICROCOLI SYSTEM, DELTAPLUSH, MODELS CPL, DPL

MICRUS MICROCOLI SYSTEM, DELTAPLUSH, MODELS CPL, DPL is an FDA 510(k)-cleared medical device (K083646) 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 January 1, 2009. Regulation: 8.