K-number	K124039
Device name	HERO GRAFT
Applicant	Hemoshpere, Inc., A Cryolife Company
Product code	DSY
Device class	Class II
Decision date	Mar 7, 2013
Decision	Substantially Equivalent
Regulation	870.3450

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Source

View the full FDA submission: accessdata.fda.gov

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HERO GRAFT

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