Xtant Medical Receives FDA Clearance of Xspan Laminoplasty Fixation System
Xtant Medical received FDA 510(k) clearance to market the Xspan™ Laminoplasty Fixation system. Initial limited launch is slated for 2Q16. ...
Xtant Medical received FDA 510(k) clearance to market the Xspan™ Laminoplasty Fixation system. Initial limited launch is slated for 2Q16. ...
Amedica has fabricated its first silicon nitride structures with a 3D printing process called robotic deposition, or robocasting....
Amendia launched the inCORPorate™ PEEK-based corpectomy device, available for thoracic and lumbar indications. ...
Precision Spine launched its Reform Modular and HA-Coated Pedicle Screw systems. Further, the company noted that 2015 was the company’s 6th consecutive year...
Implanet commenced a prospective, multicenter clinical study to document outcomes with the JAZZ Band™ implant in adult degenerative and deformity indications....
Medicrea has launched UNiD™ Lab Services, including real-time support for pre-op planning of spinal procedures, order fulfillment for the UNiD patient-specific rod...
FDAÂ is proposing to classify posterior cervical screw systems into Class II (special controls) and to continue to require premarket notification...
Wenzel Spine commenced limited launch of the VariLift®-LX system for minimally invasive lumbar fusion. Full launch is planned for spring 2016....
NuVasive received regulatory approval for ReLine™ posterior fixation technology in Japan. Launch will commence later in 2016 and continue into 2017. ...
Life Spine received FDA 510(k) clearance to market the PROLIFT® Expandable Interbody System for use in minimally invasive PLIF, TLIF and...
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