K-number	K062459
Device name	ORIGEN DBM WITH BIOACTIVE GLASS
Applicant	Nanotherapeutics
Product code	MQV
Device class	Class II
Decision date	Feb 26, 2007
Decision	Substantially Equivalent
Regulation	888.3045

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Source

View the full FDA submission: accessdata.fda.gov

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ORIGEN DBM WITH BIOACTIVE GLASS

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