Class Class II

OptiMesh Multiplanar Expandable Interbody Fusion System (K251302)

K251302 2025-12-15 Traditional
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Description

OptiMesh Multiplanar Expandable Interbody Fusion System by Spineology, Inc., an FDA 510(k) cleared orthopedic device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK251302
Clearance Date2025-12-15
Clearance TypeTraditional
Product CodeOQB
Regulation Number888.3085

Categories

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