![FDA, FTC and DOJ Enforcement of Medical Device Regulations FDA, FTC and DOJ Enforcement of Medical Device Regulations](https://www.fdanews.com/ext/resources/Book-Covers-2/BFFDEMDR-COVER.png?height=200&t=1685733565&width=200)
Home » Cook Medical’s Zenith Thoraco+ Endovascular System Designated a Breakthrough Device
Cook Medical’s Zenith Thoraco+ Endovascular System Designated a Breakthrough Device
Cook Medical’s Zenith Thoraco+ endovascular system has been designated a Breakthrough Device by the FDA.
An endovascular graft for thoracoabdominal aortic aneurysm (TAAA) patients, Thoraco+ includes four side branches for the celiac artery, superior mesenteric artery, left renal artery and right renal artery.
The Thoraco+ will be available in a range of diameters and lengths to accommodate varied patient anatomies, the Bloomington, Ind.-based company said.
Upcoming Events
-
11Jul
-
18Jul
-
21Oct