CIARTIC Move (VB10)

CIARTIC Move (VB10) is an FDA 510(k)-cleared medical device (K233748) manufactured by Siemens Medical Solutions USA, 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 March 14, 2024. Regulation: 8.