Life Spine Gains FDA Clearance for Hinged Laminoplasty System
Life Spine was granted FDA 510(k) clearance to market a Hinged Laminoplasty System....
Life Spine was granted FDA 510(k) clearance to market a Hinged Laminoplasty System....
Results from the SAKOS pivotal trial of Stryker's SpineJack® implantable fracture reduction system successfully demonstrated non-inferiority to balloon kyphoplasty (BKP), with...
Alphatec and DePuy Synthes launched interbody devices made from porous titanium....
Alphatec launched the IdentiTi TLIF Posterior Oblique Titanium Interbody Implant for transforaminal lumbar interbody fusion. ...
CarboFix received FDA 510(k) clearance to market CarboClear® Carbon Fiber fenestrated pedicle screws to treat spinal tumors. ...
Benvenue Medical, DiscGenics and Stryker shared study results for spinal technologies....
Clinical studies of Benvenue Medical's Luna interbody fusion device in minimally invasive Transforaminal Lumbar Interbody Fusion (TLIF) showed improved patient...
DePuy Synthes launched the CONDUIT Interbody Platform with 3D-printed EIT Cellular Titanium Technology....
First cases have occurred using Life Spine's PROLIFT® Lateral Expandable Spacer....
HT Medical launched additions to its line of Ti3D® cervical and lumbar interbody cages....
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