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# Intervertebral Body Graft Devices are Class 2
- URL: https://www.fdaweb.com/intervertebral-body-graft-devices-are-class-2/
- Published: 2024-09-03T12:00:00.000Z
- Updated: 2026-09-14T14:40:13.000Z
- Author: David McFarland
- Tags: FDA Policy/General, #legacy-id-D5157692

*Federal Register* notice: FDA is classifying intervertebral body graft containment devices into Class 2 (special controls). The action is based on a 2020 Spineology de novo classification request for the Spineology Interbody Fusion System. The classification describes the non-rigid implant as designed to contain the bone graft within its internal cavity. It is intended to be inserted into the intervertebral body space of the spine as an adjunct to fusion. To view the notice, click [here](https://www.govinfo.gov/content/pkg/FR-2024-09-03/pdf/2024-19726.pdf?ref=fdaweb.com).