Breakthrough for Syntellix - MAGNEZIX implant has been granted designation as a "Breakthrough Device" by the U.S. FDA

HANOVER, Germany, Oct. 30, 2020 /PRNewswire/ -- The U.S. Food & Drug Administration (FDA), Silver Spring / Maryland, has granted Syntellix's MAGNEZIX CS 3.2 device and proposed indication for use the designation of a "Breakthrough Device".