Kisar Stratford SI Screw System

Kisar Stratford SI Screw System is an FDA 510(k)-cleared medical device (K220274) manufactured by Anjali Investments L.L.C. This device is classified under the Orthopedic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on April 23, 2023. Regulation: 8.