Arrow Stiffening Stylet

Arrow Stiffening Stylet is an FDA 510(k)-cleared medical device (K220280) manufactured by Arrow International, LLC (A subsidiary of Teleflex, 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 29, 2022. Regulation: 8.