PHIN-FX Cannulated Lag Screw System

PHIN-FX Cannulated Lag Screw System is an FDA 510(k)-cleared medical device (K150693) manufactured by Ascent Medical, LLC. This device is classified under the Orthopedic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on October 12, 2015. Regulation: 8.