MODIFIED TREVO PROVUE RETRIEVER

MODIFIED TREVO PROVUE RETRIEVER is an FDA 510(k)-cleared medical device (K133464) manufactured by Concentric Medical, 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 January 16, 2014. Regulation: 8.