Arthrex Syndesmosis TightRope XP Buttress Plate Implant System

Arthrex Syndesmosis TightRope XP Buttress Plate Implant System is an FDA 510(k)-cleared medical device (K201522) 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 September 2, 2020. Regulation: 8.