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# FDA Clears Spineology’s Interbody Fusion System
- URL: https://www.fdaweb.com/fda-clears-spineologys-interbody-fusion-system/
- Published: 2017-06-27T12:00:00.000Z
- Updated: 2026-09-14T22:31:50.000Z
- Author: David McFarland
- Tags: Devices, #legacy-id-D5139034

FDA has cleared a Spineology 510(k) for the Rampart One Anterior Lumbar Interbody Fusion System. The device is designed to minimize the exposure and vascular retraction requirements associated with traditional anterior spinal fusion procedures, according to the company. It features both standard and oblique interbody device footprints each with integrated fixation screws. Spineology says Rampart One is manufactured from Invibio PEEK-OPTIMA HA Enhanced material that is intended to provide an improved osteoconductive surface for bone on-growth.