REDUCT® Headless Compression Screw System

REDUCT® Headless Compression Screw System is an FDA 510(k)-cleared medical device (K201662) manufactured by Skeletal Dynamics, 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 July 15, 2020. Regulation: 8.