K-number	K103577
Device name	TRINON Q & Q3 IMPLANT SYSTEM
Applicant	Trinon Titanium GmbH
Product code	DZE
Device class	Class II
Decision date	Jul 3, 2012
Decision	Substantially Equivalent
Regulation	872.3640

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View the full FDA submission: accessdata.fda.gov

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TRINON Q & Q3 IMPLANT SYSTEM

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