K-number	K201892
Device name	Ritleng®+ and Ritleng®+ PVP
Applicant	Fci (France Chirurgie Instrumentation) Sas
Product code	OKS
Device class	Class U
Decision date	Mar 11, 2021
Decision	Substantially Equivalent
Regulation	—

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Source

View the full FDA submission: accessdata.fda.gov

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Ritleng®+ and Ritleng®+ PVP

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