K-number	K203523
Device name	Fixone hybrid knotless anchor
Applicant	Aju Pharm Co., Ltd.
Product code	MAI
Device class	Class II
Decision date	Dec 25, 2021
Decision	Substantially Equivalent
Regulation	888.3030

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Source

View the full FDA submission: accessdata.fda.gov

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Fixone hybrid knotless anchor

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