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Abbott wins new FDA approvals for stent family including nod for next-gen Xience Skypoint

June 30, 2021 By Sean Whooley

AbbottAbbott (NYSE:ABT) announced today that the Xience stent family received FDA approval for one-month dual antiplatelet therapy (DAPT) labeling.

The FDA’s approval for one-month (as short as 28 days) DAPT labeling applies to high bleeding risk (HBR) patients in the U.S., according to a news release. The company also recently received CE mark approval in Europe for DAPT as short as 28 days, which it says gives Xience stents the shortest DAPT indication in the world.

Get the full story at our sister site, MassDevice.

Filed Under: Catheters, Tubing Components Tagged With: Abbott, fda

About Sean Whooley

Sean Whooley is an associate editor who mainly produces work for MassDevice, Medical Design & Outsourcing and Drug Delivery Business News. He received a bachelor's degree in multiplatform journalism from the University of Maryland, College Park. You can connect with him on LinkedIn or email him at swhooley@wtwhmedia.com.

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