Class Class II

Paeon Anterior Cervical Plate System, Elatus Lumbar Plate System (K223719)

K223719 2023-01-11 Special
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Description

Paeon Anterior Cervical Plate System, Elatus Lumbar Plate System by Aegis Spine, Inc. — FDA 510(k) cleared orthopedic device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK223719
Clearance Date2023-01-11
Clearance TypeSpecial
Product CodeKWQ
Regulation Number888.3060

Categories

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