Spine

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...

CoreLink introduced Scaltoff™, a stackable guide wire for the Entasis® Sacroiliac Joint Fusion system....

Stryker Spine received FDA 510(k) clearance to market the Serrato™ Pedicle Screw....

Strategic orthopaedic-related 510(k)s issued in July 2017 include: EIT Cellular Titanium Cages (EIT Emerging Implant Technologies), Lumbar Interbody System (HD LifeSciences),...

Camber Spine Technologies received FDA 510(k) clearance and commenced U.S. launch of the SPIRA™ Open Matrix ALIF device, manufactured with...