Class Class II

Arthrex VAL and VAL KreuLock™ Compression Screw System (K241592)

K241592 2024-08-31 Traditional
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Description

Arthrex VAL and VAL KreuLock™ Compression Screw System by Arthrex, Inc. — FDA 510(k) cleared orthopedic device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK241592
Clearance Date2024-08-31
Clearance TypeTraditional
Product CodeHWC
Regulation Number888.3040

Categories

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