K-number	K230537
Device name	Klassic Knee Revision System
Applicant	Total Joint Othopedics, Inc.
Product code	JWH
Device class	Class II
Decision date	May 19, 2023
Decision	Substantially Equivalent
Regulation	888.3560

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Source

View the full FDA submission: accessdata.fda.gov

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Klassic Knee Revision System

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