KASILOF Cervical Plate System

KASILOF Cervical Plate System is an FDA 510(k)-cleared medical device (K203154) manufactured by Kahtnu Surgical, 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 November 4, 2020. Regulation: 8.