On February 4, 2019, Cook Medical announced recent approval from the US Food and Drug Administration for its Zenith Dissection Endovascular System. The system consists of a proximal stent-graft component and a distal bare stent component. It provides a less invasive alternative to open surgery for repair of type B dissections. The device will be available for sale in the United States in the coming months.
Cook Medical Receives US FDA Approval for Aortic Dissection Device
Submitted by: Wei-Guo Ma
Source: Cook Medical Newsroom
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Author(s): Cook Medical
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