Tag: Cohere
Expanded FDA clearance for NuVasive’s Monolith corpectomy system
The Monolith corpectomy system (NuVasive) has been granted expanded FDA 510(k) clearance.
The system is now cleared for procedures in the cervical spine, between the...
NuVasive extends porous PEEK interbody to TLIF and PLIF procedures
NuVasive announced on 4 January the launch of the company’s Coalesce Thoracolumbar Interbody Fusion Device as well as FDA 510(k) clearance for expanded indications of...
US FDA clears Vertera Spine’s porous PEEK Coalesce LIF device
Vertera Spine has announced that the company’s Coalesce lumbar interbody fusion device has received US Food and Drug Administration (FDA) 510(k) clearance for use...
Successful early outcomes reported for Vertera Cohere fusion device
The first early successful outcomes using the Cohere cervical interbody fusion device have been reported by Vertera Spine.
Cohere is Vertera Spine's first device featuring...