K-number	K080037
Device name	MODIFICATION TO ZILVER 635 BILIARY STENT
Applicant	Cook, Inc.
Product code	FGE
Device class	Class II
Decision date	Aug 1, 2008
Decision	Unknown
Regulation	876.5010

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Source

View the full FDA submission: accessdata.fda.gov

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MODIFICATION TO ZILVER 635 BILIARY STENT

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