K-number	K213104
Device name	Auxilock Titanium Screw-In Suture Anchor
Applicant	Auxein Medical Private Limited
Product code	MBI
Device class	Class II
Decision date	Jul 29, 2022
Decision	Substantially Equivalent
Regulation	888.3040

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Source

View the full FDA submission: accessdata.fda.gov

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Auxilock Titanium Screw-In Suture Anchor

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