K-number	K160798
Device name	IPS e.max® Press Abutment Solutions for Viteo Base Ti
Applicant	Ivoclar Vivadent, AG
Product code	NHA
Device class	Class II
Decision date	Dec 15, 2016
Decision	Substantially Equivalent
Regulation	872.3630

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View the full FDA submission: accessdata.fda.gov

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IPS e.max® Press Abutment Solutions for Viteo Base Ti

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