K-number	K223438
Device name	TELIGEN System Peripheral Motor Nerve Stimulation Indications
Applicant	Medos International SARL
Product code	PDQ
Device class	Class II
Decision date	Feb 10, 2023
Decision	Substantially Equivalent
Regulation	874.1820

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View the full FDA submission: accessdata.fda.gov

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TELIGEN System Peripheral Motor Nerve Stimulation Indications

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