K-number	K030839
Device name	MEDTRONIC AVE BRIDGE AURORA BILIARY STENT SYSTEM (AURORA)
Applicant	Medtronic Ave, Inc.
Product code	FGE
Device class	Class II
Decision date	May 30, 2003
Decision	Unknown
Regulation	876.5010

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View the full FDA submission: accessdata.fda.gov

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MEDTRONIC AVE BRIDGE AURORA BILIARY STENT SYSTEM (AURORA)

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