CyberKnife Treatment Delivery System

CyberKnife Treatment Delivery System is an FDA 510(k)-cleared medical device (K170788) manufactured by Accuray Incorportaed. This device is classified under the Radiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on April 10, 2017. Regulation: 8.