WEREWOLF COBLATION System, COBLATION HALO Wand

WEREWOLF COBLATION System, COBLATION HALO Wand is an FDA 510(k)-cleared medical device (K192027) manufactured by ArthroCare Corporation. This device is classified under the General, Plastic Surgery specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on December 19, 2019. Regulation: 8.