Renovis Surgical Receives FDA Clearance for Tesera X Lateral Interbody Fusion System
Renovis Surgical received FDA 510(k) clearance to market the Tesera® X Lateral Interbody Fusion system....
Renovis Surgical received FDA 510(k) clearance to market the Tesera® X Lateral Interbody Fusion system....
Alphatec received FDA 510(k) clearance to market the OsseoScrew® expandable pedicle screw. ...
DePuy Synthes introduced SENTIO MMG, a digital system to assess nerve status and identify and avoid peripheral nerves during spine surgery....
Stryker received FDA 510(k) clearance for the SpineJack® implantable reduction system to treat osteoporotic vertebral compression fractures....
NuVasive commenced patient enrollment in a prospective, multicenter U.S. study evaluating advanced spinal implants used in XLIF® procedures....
SeaSpine commenced full launch of the Regatta® minimally invasive lateral interbody fusion system....
BlueCross BlueShield of North Dakota issued a positive commercial payor policy covering Paradigm Spine's coflex® Interlaminar Stabilization® device to treat lumbar...
Medtronic commenced U.S. launch of the Infinity OCT system for posterior cervical fusion....
Nexxt Spine commenced a clinical trial evaluating Nexxt Matrixx® 3D-printed lumbar interbody fusion devices vs. PEEK cages. ...
CoreLink Surgical launched the FLXfit®15 articulating expandable intervertebral body fusion device....
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