Spine

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....

Xtant Medical received FDA 510(k) clearance to market line extensions for the Irix-A standalone interbody spacer....

IMPLANET received FDA 510(k) clearance to market JAZZ™ Passer, a system of spinal instruments and braided band technology....

Spinal Resources received FDA 510(k) clearance to market the Swedge™ Pedicle Screw system....

NuVasive received FDA 510(k) clearance for use of redesigned MAGEC® growing rods with the RELINE® Small Stature pediatric deformity fixation system....

ChoiceSpine completed its 1,000th TOMCAT anterior cervical discectomy and fusion procedure....

Life Spine announced the first cases performed using multiple methods of in situ expansion with the PROLIFT® Lordotic system and the TiBOW™ Expandable...