K-number	K234044
Device name	ACS® LD FB Knee System
Applicant	Implantcast GmbH
Product code	JWH
Device class	Class II
Decision date	Sep 6, 2024
Decision	Substantially Equivalent
Regulation	888.3560

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Source

View the full FDA submission: accessdata.fda.gov

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ACS® LD FB Knee System

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