Arthrosurface Bone Screws

Arthrosurface Bone Screws is an FDA 510(k)-cleared medical device (K172383) 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 December 21, 2017. Regulation: 8.