Arthrosurface WristMotion Total Wrist Arthroplasty System

Arthrosurface WristMotion Total Wrist Arthroplasty System is an FDA 510(k)-cleared medical device (K200718) manufactured by Arthrosurface, 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 14, 2020. Regulation: 8.