K-number	K172036
Device name	Medrobotics Flex Robotic System
Applicant	Medrobotics Corporation
Product code	FDF
Device class	Class II
Decision date	Aug 3, 2017
Decision	Substantially Equivalent
Regulation	876.1500

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Source

View the full FDA submission: accessdata.fda.gov

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Medrobotics Flex Robotic System

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