www.fdanews.com/articles/184205-abbott-receives-ce-mark-for-xience-sierra-stent
Abbott Receives CE Mark for XIENCE Sierra Stent
November 1, 2017
Abbott received a CE Mark for its XIENCE Sierra coronary stent system.
The device helps cardiologists to access and unblock difficult-to-reach lesions. It features a thinner profile, increased flexibility, longer lengths, and small-diameters.
The company has submitted an application to the FDA for approval of the device in the United States.