Spine

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. ...

Band-LOK was allowed two U.S. patents on its proprietary Tether Clamp and Implantation System, a stabilizing bone anchor for use...

U.S. insurer Highmark now covers all U.S. FDA-cleared instrumentation for SI joint fusion, including cages or screws, with or without bone...

Interim results in a Phase IIA trial with Bone Therapeutics’ ALLOB® show evidence of successful spinal fusion and statistically significant...

K2M commenced global launch of EVEREST® Minimally Invasive XTower™ instrumentation to support the EVEREST MI XT cannulated top-loading polyaxial pedicle screw system....