Arthrex Mini Comprehensive Fixation System – 2.0mm & 2.4mm Module

Arthrex Mini Comprehensive Fixation System – 2.0mm & 2.4mm Module is an FDA 510(k)-cleared medical device (K191344) manufactured by Arthrex, Inc.. This device is classified under the Orthopedic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on October 2, 2019. Regulation: 8.