K-number	K072265
Device name	PROGENIX DMB PUTTY
Applicant	Medtronic Sofamor Danek
Product code	MQV
Device class	Class II
Decision date	Jan 9, 2008
Decision	Substantially Equivalent
Regulation	888.3045

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Source

View the full FDA submission: accessdata.fda.gov

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PROGENIX DMB PUTTY

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