K-number	K200949
Device name	HEALIX ADVANCE Anchor with DYNATAPE Suture
Applicant	Medos International SARL
Product code	MBI
Device class	Class II
Decision date	Jun 4, 2020
Decision	Substantially Equivalent
Regulation	888.3040

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Source

View the full FDA submission: accessdata.fda.gov

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HEALIX ADVANCE Anchor with DYNATAPE Suture

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