KLS Martin Cannulated Headless Screws

KLS Martin Cannulated Headless Screws is an FDA 510(k)-cleared medical device (K161259) 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 December 18, 2016. Regulation: 8.