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....
Spine Innovation announced first implantations of its Expandable TLIF device....
The German reimbursement authority renewed payment coding for 2017 for Medovex’s DenerveX™ technology for the treatment of facet joint syndrome....
Spineology received expanded FDA 510(k) clearance of the Elite Expandable Interbody Fusion system, to include a narrower 10mm version of the device and...
Results from ovine study of Bio2 Technologies’ Vitrium bioactive glass demonstrated the device’s capability to support interbody fusion....
Studies found that prevalence of CT imaging following complex spine surgery grew more than 2-fold from 6 months to 5...
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