Voyant Fine Fusion Device (EB230)

Voyant Fine Fusion Device (EB230) is an FDA 510(k)-cleared medical device (K202818) manufactured by Applied Medical. 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 15, 2021. Regulation: 8.