Class Class II

DeGen Medical Latitude-C AM Cervical Interbody Fusion System (K252737)

K252737 2025-10-10 Traditional
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Description

DeGen Medical Latitude-C AM Cervical Interbody Fusion System by Degen Medical, an FDA 510(k) cleared orthopedic device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK252737
Clearance Date2025-10-10
Clearance TypeTraditional
Product CodeODP
Regulation Number888.3080

Categories

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