Akros Scruture Anchor LisFranc Repair Kit

Akros Scruture Anchor LisFranc Repair Kit is an FDA 510(k)-cleared medical device (K200361) manufactured by Akros Medical. This device is classified under the Orthopedic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on April 5, 2020. Regulation: 8.