K-number	K062630
Device name	OSSIPRO BONE SUBSTITUTE MATERIAL
Applicant	Etex Corp.
Product code	MQV
Device class	Class II
Decision date	Jun 28, 2007
Decision	Substantially Equivalent
Regulation	888.3045

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View the full FDA submission: accessdata.fda.gov

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OSSIPRO BONE SUBSTITUTE MATERIAL

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