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# Spineology Rampart Interbody Fusion Device Cleared
- URL: https://www.fdaweb.com/spineology-rampart-interbody-fusion-device-cleared/
- Published: 2018-06-04T12:00:00.000Z
- Updated: 2026-09-15T00:10:16.000Z
- Author: David McFarland
- Tags: Devices, #legacy-id-D5141598

FDA has cleared a Spineology 510(k) for its Rampart One Standard ALIF interbody fusion system for use with or without supplemental fixation. The system includes both standard and oblique interbody devices, each with integrated fixation screws. The device is designed to minimize vascular retraction and exposure, the company says. Additionally, it is made from Invibio PEEK-Optima HA Enhanced material to support bone on-growth, it adds.