Spine Facet Replacement FDA Study Garners Best Paper Award At Lumbar Spine Research Society Meeting byTim AllenMay 3, 2024
Regulatory Spine OrthoPediatrics Corp. Receives “Breakthrough Device” Designation from FDA for eLLi™ Growing Rod System for Pediatric Patients with Scoliosis byTim AllenMay 2, 2024
Recon Regulatory Top Stories Lipogems Announces Last Patient Enrolled in the U.S. FDA IDE Arise Study for the Treatment of Knee Osteoarthritis byTim AllenApril 10, 2024
Recon Regulatory Top Stories Lipogems Announces First Patient Enrolled in the Second U.S. FDA IDE Study for the Treatment of Knee Osteoarthritis byTim AllenApril 8, 2024
Regulatory Spine Top Stories Inside information: Bioretec has been granted FDA Breakthrough Device Designation status for its RemeOs™ Spinal Interbody Cage byJosh SandbergMarch 14, 2024
Regulatory Spine FDA Grants Breakthrough Device Designation to ORTHOSON’s Bio-Structural Gel byJosh SandbergFebruary 8, 2024
Spine Top Stories 3Spine Announces Completion of FDA Clinical Trial Enrollment Achieving 325 Surgeries in 2023 byJosh SandbergJanuary 10, 2024
Biologics Spine Top Stories Biocomposites’ investee Renovos Biologics receives FDA Breakthrough Device Designation for its synthetic nanoclay bone fusion gel, RENOVITE® BMP-2 byJosh SandbergJanuary 4, 2024
Biologics Regulatory Spine Top Stories CGBio’s ‘NOVOSIS PUTTY’ Receives FDA ‘Breakthrough Device Designation,’ Accelerate Entry into the US Market byJosh SandbergJanuary 3, 2024
Biologics Regulatory MCRA Announces the Hiring of Former FDA Leadership to Advance its Regenerative Medicine Expertise byJosh SandbergNovember 15, 2023
