K-number	K220511
Device name	Medline UNITE IM Fibula Implant
Applicant	Medline Industries, LP
Product code	HWC
Device class	Class II
Decision date	Mar 22, 2022
Decision	Substantially Equivalent
Regulation	888.3040

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Source

View the full FDA submission: accessdata.fda.gov

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Medline UNITE IM Fibula Implant

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