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J Vasc Interv Radiol ; 19(7): 965-9, 2008 Jul.
Article in English | MEDLINE | ID: mdl-18672491

ABSTRACT

Expandable metal stents are used to maintain the patency of compromised ducts, lumens, and vessels. As medical devices, there products are regulated by the Center for Devices and Radiological Health of the U.S. Food and Drug Administration (FDA). During the past several years, the FDA has become aware of the increasing prevalence of off-label use of expandable metal stents cleared for biliary use within the peripheral vasculature. The authors provide an overview of how the FDA regulates medical devices and expandable stents and summarize safety issues reported to the Agency with regard to the off-label use of these biliary stents.


Subject(s)
Biliary Tract Surgical Procedures/instrumentation , Device Approval , Metals , Stents , Vascular Surgical Procedures/instrumentation , Biliary Tract Surgical Procedures/adverse effects , Biliary Tract Surgical Procedures/legislation & jurisprudence , Consumer Product Safety , Device Approval/legislation & jurisprudence , Government Regulation , Guideline Adherence , Humans , Practice Guidelines as Topic , Product Surveillance, Postmarketing , Prosthesis Design , Prosthesis Failure , United States , Vascular Surgical Procedures/adverse effects , Vascular Surgical Procedures/legislation & jurisprudence
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