Regulatory Spine Life Spine Announces FDA 510(k) Clearance for the GRUVE® + Cervical Plating System byTim AllenFebruary 18, 2025
Regulatory Spine Life Spine Announces FDA 510(k) Clearance for the ProLift® Pivot Expandable Spacer System byJosh SandbergJanuary 29, 2025
Spine Top Stories Life Spine Announces Continued Success and Industry Adoption of ProLift® Micro Endoscopic Expandable Spacer System byTim AllenOctober 16, 2024
Spine Life Spine Announces Published Article on Discectomy Performance During Transforaminal Lumbar Interbody Fusion Approach Using Endoscopic Technique vs MIS Tubular Approach byJosh SandbergSeptember 17, 2024
Spine Top Stories Life Spine Announces FDA 510(k) Clearance for the ARx® SAI Spinal Fixation System byJosh SandbergJuly 31, 2024
Regulatory Spine Top Stories Life Spine Secures Federal Court Order Permanently Prohibiting Marketing or Sale of AccelFix-XT Devices in the United States byJosh SandbergDecember 21, 2023
Spine Life Spine Releases Published Article on the Effect of Expandable Versus Static Lordotic Interbody Implants in Minimally Invasive Spine Surgery byJosh SandbergApril 18, 2023
Spine Life Spine Announces First Surgical Cases of ARx® Spinal Fixation System byJosh SandbergJanuary 5, 2023
Spine Top Stories Life Spine Announces FDA 510(K) Clearance for the TruLift® Lateral Expandable Spacer System and Lateral Plate System byJosh SandbergDecember 14, 2022
Spine Top Stories Life Spine Announces First Surgical Cases of the PROLIFT® Micro Endoscopic Expandable Spacer System byChris StewartOctober 20, 2022
