KLS Martin LINOS Wrist System

KLS Martin LINOS Wrist System is an FDA 510(k)-cleared medical device (K222624) manufactured by KLS-Martin L.P.. This device is classified under the Orthopedic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on May 24, 2023. Regulation: 8.