Captus Vascular Retrieval System

Captus Vascular Retrieval System is an FDA 510(k)-cleared medical device (K170987) manufactured by Avantec Vascular Corporation. This device is classified under the Cardiovascular specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on August 27, 2017. Regulation: 8.