For Immediate Release: February 11, 2016, PaxMed International Receives Its 180th 510(k) Submission Clearance!

On behalf of Cardinal Spine, LLC, PaxMed International, LLC receives FDA 510(k) clearance of the C-VBR vertebral body replacement device. This is a breakthrough device in that it is only the second cervical vertebral body replacement device cleared by FDA and is the first such device that has no possibility of reduction in height after surgery.