K-number	K221705
Device name	U2 Total Knee System-PF+
Applicant	United Orthopedic Corporation
Product code	MBH
Device class	Class II
Decision date	Feb 28, 2023
Decision	Substantially Equivalent
Regulation	888.3565

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Source

View the full FDA submission: accessdata.fda.gov

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U2 Total Knee System-PF+

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