K-number	K161234
Device name	CASSI II Rotational Core Biopsy System
Applicant	Scion Medical Technologies, LLC
Product code	KNW
Device class	Class II
Decision date	Aug 3, 2016
Decision	Substantially Equivalent
Regulation	876.1075

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Source

View the full FDA submission: accessdata.fda.gov

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CASSI II Rotational Core Biopsy System

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