K-number	K163018
Device name	Zilver 635 Biliary Stent
Applicant	Cook Ireland, Ltd.
Product code	FGE
Device class	Class II
Decision date	Dec 23, 2016
Decision	Unknown
Regulation	876.5010

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View the full FDA submission: accessdata.fda.gov

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Zilver 635 Biliary Stent

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