ClotTriever XL Catheter (41-102)

ClotTriever XL Catheter (41-102) is an FDA 510(k)-cleared medical device (K242557) manufactured by Inari Medical, 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 26, 2024. Regulation: 8.