K-number	K151248
Device name	PIEZOSURGERY WHITE
Applicant	Mectron S.P.A.
Product code	DZI
Device class	Class II
Decision date	Sep 4, 2015
Decision	Substantially Equivalent
Regulation	872.4120

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Source

View the full FDA submission: accessdata.fda.gov

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PIEZOSURGERY WHITE

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