K-number	K221048
Device name	Episealer Patellofemoral System
Applicant	Episurf Medical, Inc.
Product code	KRR
Device class	Class II
Decision date	Dec 23, 2022
Decision	Substantially Equivalent
Regulation	888.3540

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Source

View the full FDA submission: accessdata.fda.gov

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Episealer Patellofemoral System

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