K-number	K081784
Device name	MASTERGRAFT PUTTY
Applicant	Medtronic Sofamor Danek
Product code	LYC
Device class	Class II
Decision date	Sep 17, 2008
Decision	Substantially Equivalent
Regulation	872.3930

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Source

View the full FDA submission: accessdata.fda.gov

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MASTERGRAFT PUTTY

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