K-number	K130216
Device name	ATLANTIS STRAUMANN BONE LEVEL ABUTMENT
Applicant	Dentsply Implant
Product code	NHA
Device class	Class II
Decision date	May 1, 2013
Decision	Substantially Equivalent
Regulation	872.3630

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Source

View the full FDA submission: accessdata.fda.gov

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ATLANTIS STRAUMANN BONE LEVEL ABUTMENT

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