Spine

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....

HD LifeSciences received FDA 510(k) clearance and commenced U.S. launch of NanoHive™, a system of interbody devices for ALIF, PLIF and...

Providence Medical Technology received FDA 510(k) clearance to market the ALLY™ Posterior Fixation system as an adjunct to fusion in the...

Stryker’s Serrato™ Pedicle Screws have been implanted by >100 U.S. surgeons during the first 30 days of initial launch....

Paradigm Spine announced issuance of a Blue Cross Blue Shield of Michigan Medical Policy that brings coverage of the coflex® Interlaminar...

SeaSpine commenced full commercial launch of Shoreline®, its anterior cervical standalone system....

Stryker Spine received FDA 510(k) clearance to market its 3D-printed Tritanium® C Anterior Cervical Cage. ...