K-number	K142221
Device name	MEMO 3D ReChord
Applicant	Sorin Group Italia S.R.L.
Product code	KRH
Device class	Class II
Decision date	Aug 29, 2014
Decision	Substantially Equivalent
Regulation	870.3800

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View the full FDA submission: accessdata.fda.gov

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MEMO 3D ReChord

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