Spine

Alphatec Spine launched and completed initial procedures with the Battalion™ Lateral System and Squadron™ Lateral Retractor....

The U.K.’s National Institute for Health and Care Excellence published guidance recommending availability of minimally invasive sacroiliac joint fusion surgery to...

Aesculap Implant Systems established a warranty program for its Plasmapore®XP-coated spinal interbody fusion devices, and launched the TSpace®XP interbody system....

SI-BONE’s iFuse Implant System® for SI joint fusion has been used in >25,000 procedures worldwide....

Providence Medical Technology received FDA 510(k) clearance for ALLY™ Facet Screws and for standalone use of the CAVUX™ Cervical Cage-L system....

NuVasive received FDA 510(k) clearance to market the CoRoent® Small Interbody™ System for intervertebral body fusion at multiple contiguous levels in...

Spineway announced completion of the first minimally invasive surgery in the U.S. using the Mont Blanc MIS line....

Spinal Elements announced successful completion of initial procedures using the Lucent® XP expandable interbody device....

NuVasive announced updated guidance from the National Industry for Clinical Excellence in the U.K. for lateral lumbar interbody fusion. ...

Medtronic received FDA 510(k) clearance of Kyphon™ Xpede Bone Cement for fixation of pathological fractures of the sacral ala using sacroplasty....