Spine

CoreLink received FDA 510(k) clearance to market the Foundation 3D Anterior Lumbar Interbody Fusion device....

Zavation commenced launch of its Facet screw and Sacroiliac screw systems....

Centinel Spine announced UnitedHealthcare's positive medical policy for Lumbar Total Disc Replacement, granting 16MM patients access to the prodisc® L device....

OrthoPediatrics announced an additional FDA 510(k) clearance for the FIREFLY® Pedicle Screw Navigation Guide to include S2AI screw trajectory for sacral-iliac fixation...

CarboFix Orthopedics received FDA 510(k) clearance to market the CarboClear® Carbon Fiber Pedicle Screw to treat oncological patients....

DePuy Synthes commenced U.S. launch of the CONCORDE LIFT Expandable Interbody, part of the UNLEASH MIS TLIF Procedural Solution....

FBC Device received its first FDA 510(k) clearance, granted for the FBC 921 ALIF interbody implant....

Results from an efficacy study of ReVivo Medical's spinal fusion technology demonstrated that loadsharing through elastic micro-motion accelerates bone formation and...

HAPPE Spine has formed to develop technology that supports construction of partial or fully porous hydroxyapatite-reinforced PEEK implants. ...

NuVasive commenced U.S. launch of MAGEC X, an extension of its MAGEC line to treat Early Onset Scoliosis. ...