K-number	K211671
Device name	Journey II Mid-Level Tibial Inserts
Applicant	Smith & Nephew, Inc.
Product code	JWH
Device class	Class II
Decision date	Aug 17, 2021
Decision	Substantially Equivalent
Regulation	888.3560

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Source

View the full FDA submission: accessdata.fda.gov

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Journey II Mid-Level Tibial Inserts

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