February 2026 Medtronic received U.S. FDA approval for expanded labeling of Infuse™ Bone Graft with compatible spinal fixation systems for transforaminal lumbar interbody fusion (TLIF), strengthening its spinal surgery portfolio that supports complex spinal deformity procedures, including selected scoliosis-related interventions.
October 2025 The U.S. FDA's Pediatric Advisory Committee reviewed post-market safety data for Globus Medical's REFLECT™ Scoliosis Correction System, supporting continued post-approval evaluation through a multicenter U.S. registry for skeletally immature patients with idiopathic scoliosis.