Voyager Trajectory Array Guide (V-TAG)

Voyager Trajectory Array Guide (V-TAG) is an FDA 510(k)-cleared medical device (K180854) manufactured by Voyager Therapeutics, 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 July 22, 2018. Regulation: 8.