Tag: Vertera Spine
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...
NuVasive acquires Vertera Spine
NuVasive has announced the company's acquisition of Vertera Spine, a privately-held medical device company developing and commercialising interbody implants for spinal fusion using patented...
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...
US CMS issues new code to track use of radiolucent porous...
The US Centers for Medicare & Medicaid Services (CMS) has issued a new ICD-10 code (10th revision of the International Statistical Classification of Diseases...
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...