Crosser iQ CTO Recanalization System

Crosser iQ CTO Recanalization System is an FDA 510(k)-cleared medical device (K203363) manufactured by C.R. Bard, 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 August 11, 2021. Regulation: 8.