K-number	K131557
Device name	RITTER IMPLANT SYSTEM
Applicant	Ritter Implants GmbH CO KG
Product code	DZE
Device class	Class II
Decision date	May 9, 2014
Decision	Substantially Equivalent
Regulation	872.3640

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Source

View the full FDA submission: accessdata.fda.gov

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RITTER IMPLANT SYSTEM

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