Endoluminal Occlusion System, EOS-X, Endoluminal Occlusion System, EOS

Endoluminal Occlusion System, EOS-X, Endoluminal Occlusion System, EOS is an FDA 510(k)-cleared medical device (K212057) manufactured by Artventive Medical Group, Inc.. This device is classified under the Cardiovascular specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on February 28, 2022. Regulation: 8.