First Ray Receives FDA 510(k) Clearance for CortiClamp Small Bone Fixation System
First Ray received FDA 510(k) clearance for the CortiClamp™ System for small bone fixation. ...
May 16, 2016,
First Ray Receives FDA 510(k) Clearance for CortiClamp Small Bone Fixation System
Xtant Medical Receives FDA Clearance for Posterior Cervical Screw Indication on Certex Spinal Fixation
Xtant Medical received FDA 510(k) clearance of a posterior cervical screw indication for the Certex® Spinal Fixation system....
May 13, 2016, Julie Vetalice
Tecres and Keensight to Form Demetra
Demetra Holding has formed with investment from Tecres and Keensight, which acquired aap Implantate’s biomaterials assets. ...
May 12, 2016, Julie Vetalice
Initial Cases Performed with Life Spine PROLIFT Expandable Interbody System
Life Spine announced successful completion of initial cases with the PROLIFT® Expandable Interbody System for minimally invasive PLIF, TLIF and...
May 12, 2016, Julie Vetalice
Strategic Orthopaedic-related 510(k)s issued in April 2016
Strategic orthopaedic-related 510(k)s issued in April 2016 include: Olympic Posterior Spinal Fixation System (Astura Medical); Revival Modular Revision Hip Stem (Corin);...
May 11, 2016, Julie Vetalice
aap Implantate Completes Sale of Biomaterials Unit
aap Implantate completed the sale of its aapBiomaterials subsidiary. The buyer is Keensight Capital....
May 11, 2016, Julie Vetalice
100 Surgeries with ROSA Spine
Medtech announced that 100 spinal surgeries have been successfully performed with the ROSA™ Spine robotic-assistive device for minimally invasive surgery....
May 11, 2016, Julie Vetalice
OrthoPediatrics Enters Japan Market
OrthoPediatrics received Japan regulatory clearance for RESPONSE™ Spine for use in pediatric and adult patients. The product will be distributed...
May 11, 2016, Julie Vetalice
First Surgeries with Safe Orthopaedics’ SteriSpineCC Range
Safe Orthopaedics confirmed initial successful surgeries using SteriSpine™CC devices, for use in the cervical spine. Full launch is planned for...
May 11, 2016, Julie Vetalice
Camber Spine Receives FDA Clearance for ENZA Zero Profile ALIF Device
Camber Spine Technologies received FDA 510(k) clearance to market the ENZA™ Zero Profile Anterior Interbody Fusion system....
May 10, 2016, Julie Vetalice
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