Spine

DePuy Synthes unveiled the VIPER PRIME™ pedicle screw. Full EMEA commercial launch is slated for early 2018....

NuVasive received expanded FDA 510(k) clearance of the TLX™ interbody fusion system, including an expandable 20° cage, use with allogeneic bone graft and...

ChoiceSpine received FDA 510(k) clearance to market the HAWKEYE Ti vertebral body replacement, its first 3D-printed device....

4WEB Medical launched its next-generation 3D-printed Anterior Spine Truss interbody fusion system....

Nexxt Spine received FDA 510(k) clearance to market 3D-printed NEXXT MATRIXX™ interbody and vertebral body replacement devices. ...

Spineology commenced full market release of the Elite™ Expandable Interbody Fusion system. More than 300 cases have been completed since limited...

Zimmer Biomet commenced U.S. launch of the Avenue® T TLIF Cage, featuring self-guided, curved VerteBRIDGE® plating....

K2M received FDA 510(k) clearance to market the YUKON™ OCT system to support fusion with posterior fixation in the occipito-cervico-thoracic spine. ...

Wenzel Spine commenced U.S. launch of revisions to its VariLift®-C standalone interbody fusion system, including new implant sizes and MIS instrumentation. ...

Expanding Orthopedics received FDA 510(k) clearance for the FLXfit™15 expandable interbody cage....