Spineology Receives FDA Clearance for Rampart One Anterior Lumbar Interbody Fusion System

By Julie A. Vetalice

Spineology announced FDA clearance of the Rampart One Anterior Lumbar Interbody Fusion System. This marks the company’s first product clearance in the anterior market.

Rampart One is designed to minimize the exposure and vascular retraction requirements associated with traditional anterior fusion. The system includes standard and oblique interbody device footprints with integrated fixation screws and is manufactured from Invibio® PEEK-OPTIMA® HA Enhanced polymer.

Rampart One follows clearance of Spineology’s expandable interbody fusion system in March.

Sources: Spineology; ORTHOWORLD Inc.

Photo courtesy of Spineology

Product Labels: Spinal Fusion

Tags: 510(k) Clearance, Regulatory