K-number	K060306
Device name	ACCELL CONNEXUS DEMINERALIZED BONE MATRIX PUTTY
Applicant	Isotis NV
Product code	NUN
Device class	Class II
Decision date	Mar 27, 2006
Decision	Substantially Equivalent
Regulation	872.3930

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View the full FDA submission: accessdata.fda.gov

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ACCELL CONNEXUS DEMINERALIZED BONE MATRIX PUTTY

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