Spine

Tenon Medical received FDA 510(k) clearance to market the Catamaran Sacroiliac Joint Fixation system, indicated for sacroiliac joint fusion to treat...

Study results indicate that NuVasive's porous PEEK technology, used in the Cohere® cervical interbody fusion device, presents a clinically viable option to...

Medtronic gained FDA 510(k) clearance for Kyphon HV-R Bone Cement for use in sacroplasty....

OrthoPediatrics marked the first spine surgery in Japan with the RESPONSE spine system....

Globus Medical launched the CREO® Fenestrated Screw, designed for use with FORTRESS bone cement to treat thoracolumbar spinal tumors....

RTI Surgical launched Fortilink®-TS and -L lumbar interbody fusion systems, which feature TETRAfuse® 3D printed polymer....

Medacta announced the first surgery performed in the U.S. using the Medacta Unconstrained Screw Technology Sacro-Iliac Joint Screw (M.U.S.T. SI) for sacroiliac...

Centinel Spine received FDA 510(k) clearance to market the FLX platform of Integrated Interbody and non-integrated interbody fusion devices....

K2M achieved the milestone of its 100th product following FDA 510(k) clearance and launch of the OZARK Cervical Plate....

Spineology received FDA 510(k) clearance to market the Rampart One Standard ALIF device without supplemental fixation....