K-number	K211221
Device name	Porous Patella and Porous Tibia Baseplate
Applicant	Smith & Nephew, Inc.
Product code	MBH
Device class	Class II
Decision date	Oct 1, 2021
Decision	Substantially Equivalent
Regulation	888.3565

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Source

View the full FDA submission: accessdata.fda.gov

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Porous Patella and Porous Tibia Baseplate

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