K-number	K200888
Device name	OMNIBotics Knee System
Applicant	Corin, Ltd.
Product code	OLO
Device class	Class II
Decision date	Jun 27, 2020
Decision	Substantially Equivalent
Regulation	882.4560

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Source

View the full FDA submission: accessdata.fda.gov

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OMNIBotics Knee System

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