K-number	K113539
Device name	REVOIS PRO IMPLANT STSYEM
Applicant	Riemser Arzneimittel AG
Product code	DZE
Device class	Class II
Decision date	May 3, 2013
Decision	Substantially Equivalent
Regulation	872.3640

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Source

View the full FDA submission: accessdata.fda.gov

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REVOIS PRO IMPLANT STSYEM

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