K-number	K203479
Device name	ExtremiLOCK Lateral Ankle Fusion Plates
Applicant	Osteomed
Product code	HRS
Device class	Class II
Decision date	Feb 24, 2021
Decision	Substantially Equivalent
Regulation	888.3030

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Source

View the full FDA submission: accessdata.fda.gov

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ExtremiLOCK Lateral Ankle Fusion Plates

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