Vy Spine ClariVy Cervical IBF System

Vy Spine ClariVy Cervical IBF System is an FDA 510(k)-cleared medical device (K212715) manufactured by Vy Spine, LLC. This device is classified under the Orthopedic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on December 19, 2021. Regulation: 8.