K-number	K103020
Device name	ATLANTIS ABUTMENT FOR KEYSTONE IMPLANT, ATLANTIS GEMINI ABUTMENT
Applicant	Atlantis Components, Inc.
Product code	NHA
Device class	Class II
Decision date	Feb 3, 2011
Decision	Substantially Equivalent
Regulation	872.3630

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View the full FDA submission: accessdata.fda.gov

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ATLANTIS ABUTMENT FOR KEYSTONE IMPLANT, ATLANTIS GEMINI ABUTMENT

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