K-number	K153667
Device name	TRUESPAN Meniscal Repair System
Applicant	Medos International SARL
Product code	MBI
Device class	Class II
Decision date	Mar 24, 2016
Decision	Substantially Equivalent
Regulation	888.3040

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Source

View the full FDA submission: accessdata.fda.gov

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TRUESPAN Meniscal Repair System

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