FMS VUE™ Fluid Management and Tissue Debridement System

FMS VUE™ Fluid Management and Tissue Debridement System is an FDA 510(k)-cleared medical device (K233675) manufactured by DePuy Mitek, Inc.. This device is classified under the Orthopedic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on February 25, 2024. Regulation: 8.