K-number	K100785
Device name	BONART MODEL ART-IM1 IMPLANTOR SYSTEM & ACCESSORIES
Applicant	Bonart Co., Ltd.
Product code	EBW
Device class	Class I
Decision date	Dec 3, 2010
Decision	Substantially Equivalent
Regulation	872.4200

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View the full FDA submission: accessdata.fda.gov

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BONART MODEL ART-IM1 IMPLANTOR SYSTEM & ACCESSORIES

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