K-number	K143051
Device name	ArgenIS Titanium Abutments
Applicant	The Argen Corporation
Product code	NHA
Device class	Class II
Decision date	Sep 16, 2015
Decision	Substantially Equivalent
Regulation	872.3630

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Source

View the full FDA submission: accessdata.fda.gov

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ArgenIS Titanium Abutments

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