Spine

Amedica submitted its responses to FDA in relation to the CASCADE clinical trial, and expects a final determination from FDA within 60 days. ...

Titan Spine is amending its device warranty to provide a free replacement if any Endoskeleton® interbody fusion devices delaminate or generate...

SI-BONE received FDA 510(k) clearance of a modified indication for the iFuse Implant System®, noting that clinical studies have demonstrated its ability...

As of 2Q15, >15,000 of Spineart’s BAGUERA® C cervical disc replacement devices have been successfully implanted worldwide....

Vertera Spine announced first implantations with the COHERE™ Cervical Interbody Fusion system. Full market launch is expected in coming months....

LDR announced initial implantations of the ROI-C® Titanium-Coated Cervical Cage....

Life Spine announced successful completion of initial cases with the PLATEAU®-Ti Spacer, a titanium interbody system featuring OSSEO-LOC™ surface treatment to support potential...

Eden Spine received CE Mark approval for the SPHYNX™ titanium plate to treat thoracolumbar instability....

Pinnacle Spine launched the InFill® Anterior Lumbar Interbody Fusion device, compatible with the InFill Graft Delivery System....

K2M received FDA 510(k) clearances to market CASCADIA™ Cervical and CASCADIA AN Lordotic Oblique Interbody systems, featuring Lamellar 3D-printed Titanium Technology™....