Class Class II

Titanium Interbody System (K253266)

K253266 2026-01-08 Special
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Description

Titanium Interbody System by Spine Innovation, LLC, an FDA 510(k) cleared orthopedic device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK253266
Clearance Date2026-01-08
Clearance TypeSpecial
Product CodeMAX
Regulation Number888.3080

Categories

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