K-number	K242554
Device name	Arthrex VAL and VAL KreuLock Compression Screw System
Applicant	Arthrex, Inc.
Product code	HRS
Device class	Class II
Decision date	Oct 21, 2024
Decision	Substantially Equivalent
Regulation	888.3030

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Source

View the full FDA submission: accessdata.fda.gov

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Arthrex VAL and VAL KreuLock Compression Screw System

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Arthrex VAL and VAL KreuLock Compression Screw System