Regulatory Spine SI-BONE, Inc. Receives 510(k) Clearance and FDA Breakthrough Device Designation for Pelvic Fracture Fixation System byJosh SandbergAugust 20, 2024
Regulatory Spine MiRus Receives Breakthrough Device Designation for Spine Implant byJosh SandbergAugust 1, 2024
Spine Canary Medical’s Smart Spine Lumbar Cartridge Granted FDA “Breakthrough Device” Designation byTim AllenMay 29, 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
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
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
Recon Regulatory ZKR Orthopedics announces FDA Breakthrough Device designation for the LIFT Implant Technology byJosh SandbergOctober 10, 2023
Regulatory Spine FDA Grants Second Breakthrough Device Designation for Carlsmed Technology byJosh SandbergSeptember 20, 2023
