PercuNav Image Fusion and Interventional Navigation System

PercuNav Image Fusion and Interventional Navigation System is an FDA 510(k)-cleared medical device (K223804) manufactured by Philips Ultrasound, LLC. This device is classified under the Radiology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on January 17, 2023. Regulation: 8.