K-number	K180759
Device name	SECULOK Suture Anchor
Applicant	U&I Corporation
Product code	MBI
Device class	Class II
Decision date	Aug 9, 2018
Decision	Substantially Equivalent
Regulation	888.3040

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Source

View the full FDA submission: accessdata.fda.gov

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SECULOK Suture Anchor

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SECULOK Suture Anchor