ALTSTAETTEN, Switzerland, June 12, 2018 /PRNewswire/ — icotec AG, a Swiss company, today announced that its latest line of interbody cages, designed to optimize bony integration and post-operative visualization has received U.S. Food and Drug Administration (FDA) 510(k) clearance. The clearance includes cages for a variety of surgical approaches, such as cervical fusion procedures like Anterior Cervical Discectomy […]

Share on LinkedInShare on FacebookShare on Google+Pin on PinterestEmail this to someone