K-number	K102531
Device name	MUCOGRAFT
Applicant	Ed. Geistlich Soehne AG Fur Chemische Industrie
Product code	NPL
Device class	Class II
Decision date	Nov 17, 2010
Decision	Substantially Equivalent
Regulation	872.3930

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View the full FDA submission: accessdata.fda.gov

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MUCOGRAFT

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