Cardinal Spine Receives FDA 510(k) Clearance for Cervical Vertebral Body Replacement

On behalf of Cardinal Spine, PaxMed International received FDA 510(k) clearance of the C-VBR vertebral body replacement—reportedly the second cervical vertebral body replacement device to be cleared by FDA and the first such device designed with no possibility of reduction in height after surgery.

Source: PaxMed International

 
...

document icon

You are out of free articles for this month

Subscribe as a Guest for $0 and unlock a total of 5 articles per month.

You are out of five articles for this month

Subscribe as an Executive Member for access to unlimited articles, THE ORTHOPAEDIC INDUSTRY ANNUAL REPORT and more.

JV

Julie Vetalice is ORTHOWORLD's Editorial Assistant. She has covered the orthopedic industry for over 20 years, having joined the company in 1999.



Contact Us

0