OQB · Class II · 21 CFR 888.3085

Intervertebral Body Graft Containment Device — FDA 510(k) Devices

An Intervertebral Body Graft Containment Device Is A Non-rigid, Implanted Spinal Device That Is Designed To Contain Bone Graft Within Its Internal Cavity. The Device Is Inserted Into The Intervertebral Body Space Of The Spine And Is Intended As An Adjunct To Intervertebral Body Fusion.

3
Total
3
Cleared
189d
Avg days
2023
Since

List of Intervertebral Body Graft Containment Device devices cleared through 510(k)

3 devices
1–3 of 3

How to use this database

This page lists all FDA 510(k) submissions for Intervertebral Body Graft Containment Device devices (product code OQB). Click any device to view full submission details, including the decision date, manufacturer information, predicate device, and a link to the official FDA record.

These devices fall under the Orthopedic FDA review panel. Browse all Orthopedic devices →