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Intervertebral Body Graft Containment Device

FDA product code OQB · Class 2 · Orthopedic

21

Registered devices

28

Adverse events

0

Recalls

4

510(k) clearances

Devices with this code

Dual Chamber Expandable Interbody Fusion System — SPINEOLOGY INC.OptiMesh Multiplanar Expandable Interbody Fusion System — SPINEOLOGY INC.Dual Chamber Expandable Interbody Fusion System — SPINEOLOGY INC.OptiMesh Expandable Interbody Fusion System — SPINEOLOGY INC.OptiMesh Expandable Interbody Fusion System — SPINEOLOGY INC.OptiMesh Multiplanar Expandable Interbody Fusion System — SPINEOLOGY INC.OptiMesh Expandable Interbody Fusion System — SPINEOLOGY INC.OptiMesh Expandable Interbody Fusion System — SPINEOLOGY INC.OptiMesh Expandable Interbody Fusion System — SPINEOLOGY INC.OptiMesh HA Nano Multiplanar Expandable Interbody Fusion System — SPINEOLOGY INC.OptiMesh Expandable Interbody Fusion System — SPINEOLOGY INC.OptiMesh Expandable Interbody Fusion System — SPINEOLOGY INC.OptiMesh Expandable Interbody Fusion System — SPINEOLOGY INC.OptiMesh Multiplanar Expandable Interbody Fusion System — SPINEOLOGY INC.Diverted Bone Tube — SPINEOLOGY INC.OptiMesh HA Nano Multiplanar Expandable Interbody Fusion System — SPINEOLOGY INC.OptiMesh HA Nano Multiplanar Expandable Interbody Fusion System — SPINEOLOGY INC.OptiMesh Expandable Interbody Fusion System — SPINEOLOGY INC.OptiMesh HA Nano Multiplanar Expandable Interbody Fusion System — SPINEOLOGY INC.OptiMesh Multiplanar Expandable Interbody Fusion System — SPINEOLOGY INC.OptiMesh Multiplanar Expandable Interbody Fusion System — SPINEOLOGY INC.

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