K-number	K192709
Device name	Fixone All Suture Anchor
Applicant	Aju Pharm Co., Ltd.
Product code	MBI
Device class	Class II
Decision date	Dec 15, 2020
Decision	Substantially Equivalent
Regulation	888.3040

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Source

View the full FDA submission: accessdata.fda.gov

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Fixone All Suture Anchor

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