FlowTriever Retrieval/Aspiration System, Aspiration Guide Catheter

FlowTriever Retrieval/Aspiration System, Aspiration Guide Catheter is an FDA 510(k)-cleared medical device (K173672) manufactured by Inari Medical. This device is classified under the Cardiovascular specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on February 4, 2018. Regulation: 8.