K-number	K231326
Device name	Fix2Lock(Biocomposite medial, lateral, Biocombi Self Punching)
Applicant	Osteonic Co., Ltd.
Product code	MAI
Device class	Class II
Decision date	May 31, 2023
Decision	Substantially Equivalent
Regulation	888.3030

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View the full FDA submission: accessdata.fda.gov

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Fix2Lock(Biocomposite medial, lateral, Biocombi Self Punching)

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