Class Class II

Luna® Ti Interbody Fusion System (K250773)

K250773 2026-02-04 Traditional
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Description

Luna® Ti Interbody Fusion System by Spinal Elements, Inc., an FDA 510(k) cleared orthopedic device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK250773
Clearance Date2026-02-04
Clearance TypeTraditional
Product CodeMAX
Regulation Number888.3080

Categories

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