VERASENSE for Zimmer Biomet Persona

VERASENSE for Zimmer Biomet Persona is an FDA 510(k)-cleared medical device (K180459) manufactured by Orthosensor, Inc.. This device is classified under the Neurology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on June 6, 2018. Regulation: 8.