K-number	K191459
Device name	JuggerStitch Meniscal Repair Device
Applicant	Biomet, Inc.
Product code	MBI
Device class	Class II
Decision date	Sep 13, 2019
Decision	Substantially Equivalent
Regulation	888.3040

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Source

View the full FDA submission: accessdata.fda.gov

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JuggerStitch Meniscal Repair Device

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