AZUR CX Detachable 18 Peripheral Coil System

AZUR CX Detachable 18 Peripheral Coil System is an FDA 510(k)-cleared medical device (K162524) manufactured by MicroVention, Inc.. 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, 2017. Regulation: 8.