K-number	K122585
Device name	CRUX VENA CAVA FILTER SYSTEM
Applicant	Crux Biomedical
Product code	DTK
Device class	Class II
Decision date	Jan 17, 2013
Decision	Substantially Equivalent
Regulation	870.3375

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Source

View the full FDA submission: accessdata.fda.gov

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CRUX VENA CAVA FILTER SYSTEM

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