Class Class II

F3D Interbody System (K230329)

K230329 2023-06-06 Traditional
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Description

F3D Interbody System by Corelink, LLC — FDA 510(k) cleared orthopedic device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK230329
Clearance Date2023-06-06
Clearance TypeTraditional
Product CodeODP
Regulation Number888.3080

Categories

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