Orthofix Announces FDA Clearance, Limited Launch of FORZA PTC Interbody Spacer

Orthofix announced FDA 510(k) clearance and U.S. limited launch of the FORZA® PTC™ (Peek Titanium Composite) Spacer.

Xtant Medical Receives FDA Clearance for Posterior Cervical Screw Indication on Certex Spinal Fixation

Xtant Medical received FDA 510(k) clearance of a posterior cervical screw indication for the Certex® Spinal Fixation system.

Initial Cases Performed with Life Spine PROLIFT Expandable Interbody System

Life Spine announced successful completion of initial cases with the PROLIFT® Expandable Interbody System for minimally invasive PLIF, TLIF and oblique approaches. 

OrthoPediatrics Enters Japan Market

OrthoPediatrics received Japan regulatory clearance for RESPONSE™ Spine for use in pediatric and adult patients. The product will be distributed regionally through an exclusive agreement with Robert Reid.