Positive Comparative Data from 7-Year Follow-Up Study of Mobi-C

Seven-year outcomes study data demonstrated statistical superiority of Zimmer Biomet’s Mobi-C® Cervical Disc vs. 2-level ACDF in overall success. 

NuVasive Secures Magnetic Resonance FDA Conditional Clearance for MAGEC

NuVasive received FDA clearance for magnetic resonance imaging under certain conditions on patients treated with the MAGEC® growth modulation system.

DePuy Synthes Launches SYNFIX Evolution for ALIF

DePuy Synthes Spine launched SYNFIX® Evolution for standalone Anterior Lumbar Interbody Fusion (ALIF). 

SeaSpine Receives FDA 510(k) Clearance for Shoreline ACS System

SeaSpine received FDA 510(k) clearance to market the Shoreline™ ACS Anterior Cervical Standalone system. Full commercial launch is slated for 1H17.

4WEB Medical Announces First U.S. Surgeries with Curved TLIF Device

4WEB Medical announced completion of first surgeries using the Curved Posterior Spine Truss system for TLIF procedures. 

Tyber Medical Launches TyPEEK Lateral Implant

Tyber Medical commenced full launch of their lateral access, next-gen lateral PEEK/titanium composite interbody and lateral plating systems.

RTI Surgical Receives Additional 510(k) Clearance for Streamline OCT System

RTI Surgical received an expanded FDA 510(k) clearance for the Streamline OCT Occipito-Cervico-Thoracic System, including an indication for polyaxial screw placement in the cervical spine, and also clearance for a dual diameter transition rod.