Class Class II

PreView-III™ Anterior Cervical Plate System (K223627)

K223627 2023-02-02 Traditional
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Description

PreView-III™ Anterior Cervical Plate System by Nexus Spine, LLC — FDA 510(k) cleared orthopedic device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK223627
Clearance Date2023-02-02
Clearance TypeTraditional
Product CodeKWQ
Regulation Number888.3060

Categories

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