VerteGlide Spinal Growth Guidance System

VerteGlide Spinal Growth Guidance System is an FDA 510(k)-cleared medical device (K241816) manufactured by OrthoPediatrics Corp.. This device is classified under the Orthopedic specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on March 13, 2025. Regulation: 8.