AXS Vecta Aspiration System

AXS Vecta Aspiration System is an FDA 510(k)-cleared medical device (K190212) manufactured by Stryker Neurovascular. This device is classified under the Cardiovascular specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on April 23, 2019. Regulation: 8.