Vy Spine™ VyLam™ Laminoplasty System

Vy Spine™ VyLam™ Laminoplasty System is an FDA 510(k)-cleared medical device (K232471) 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 October 9, 2023. Regulation: 8.