K-number	K201436
Device name	Vortek Single Loop Ureteral Stent
Applicant	Coloplast Corp.
Product code	FAD
Device class	Class II
Decision date	Feb 25, 2021
Decision	Substantially Equivalent
Regulation	876.4620

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Source

View the full FDA submission: accessdata.fda.gov

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Vortek Single Loop Ureteral Stent

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