FDA to Consider Expanding Indication for Carotid Stenting to Standard-Risk
Surgical Patients
JANUARY 2011 | Should patients at standard risk for adverse events from carotid endarterectomy be treated with carotid artery stenting? That
is the question a Food and Drug Administration (FDA) advisory panel will grapple with this Wednesday as panel members gather to make recommendations and vote
on an expanded indication for the RX Acculink Carotid Stent System (Abbott, Abbott Park, IL). Source: heartwire/Medscape.com Read the article»
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INTERSOCIETAL ACCREDITATION COMMISSION
CAROTID STENTING | ICACSF
6021 University Boulevard, Suite 500, Ellicott City, MD 21043
800.838.2110 phone | 888.806.7519 fax | www.intersocietal.org/carotid
