Spine

Medovex received CE Mark approval for the DenerveX™ system....

Prosidyan received FDA 510(k) clearance of FIBERGRAFT BG Putty for use in posterolateral spinal fusion. ...

Zimmer Biomet is recalling SpF® PLUS-Mini and SpF XL IIb Implantable Spinal Fusion Stimulators due to potential cytotoxicity issues that were...

K2M launched MESA 2 Cricket™ instrumentation, an enhancement to the MESA® 2 pedicle screw system. ...

VEXIM received regulatory approval from ANVISA to commercialize SpineJack® in Brazil....

NuVasive is increasing investment in support of adult/pediatric spinal deformity research and education, and expects to launch the RELINE® Small...

Life Spine announces the approval of a study to help determine optimal outcomes for Open vs. Minimally Invasive Posterior Lumbar...

Life Spine commenced full commercial launch of the PROLIFT® Lordotic expandable interbody system with OSSEO-LOC™ surface treatment....

Vertebral Technologies received notice of allowance for its patent, "Methods and Apparatus for Minimally Invasive Modular Interbody Fusion Devices."...

Life Spine received FDA 510(k) clearance of its CRANIAL FUSION system, expanding indications for use of SOLSTICE Polyaxial Screws into...