PercuNav Image Fusion and Interventional Navigation

PercuNav Image Fusion and Interventional Navigation is an FDA 510(k)-cleared medical device (K170716) manufactured by Philips Ultrasound, Inc.. 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 20, 2017. Regulation: 8.