K-number	K180057
Device name	VORTEK URETERAL DOUBLE LOOP STENT
Applicant	Coloplast Corp.
Product code	FAD
Device class	Class II
Decision date	Mar 9, 2018
Decision	Substantially Equivalent
Regulation	876.4620

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Source

View the full FDA submission: accessdata.fda.gov

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VORTEK URETERAL DOUBLE LOOP STENT

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