Class Class II

ATEC Lateral Plate System (K230721)

K230721 2023-05-09 Traditional
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Description

ATEC Lateral Plate System by Alphatec Spine, Inc. — FDA 510(k) cleared orthopedic device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK230721
Clearance Date2023-05-09
Clearance TypeTraditional
Product CodeKWQ
Regulation Number888.3060

Categories

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