CrossFAST™ Integrated Microcatheter Guide Extension System (CFM55)

CrossFAST™ Integrated Microcatheter Guide Extension System (CFM55) is an FDA 510(k)-cleared medical device (K242276) manufactured by Vantis Vascular, 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 September 29, 2024. Regulation: 8.