K-number	K060794
Device name	PROGENIX DBM PUTTY AND PASTE
Applicant	Medtronic Sofamor Danek
Product code	MBP
Device class	Class II
Decision date	Dec 18, 2006
Decision	Substantially Equivalent
Regulation	888.3045

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Source

View the full FDA submission: accessdata.fda.gov

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PROGENIX DBM PUTTY AND PASTE

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