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HomeFDASpineology® Announces FDA Clearance of Rampart One™ Anterior Lumbar Interbody Fusion System

Spineology® Announces FDA Clearance of Rampart One™ Anterior Lumbar Interbody Fusion System

Spineology, Inc. the innovator in anatomy-conserving surgery™, announced FDA clearance of their Rampart One Anterior Lumbar Interbody Fusion System.

Design:  Rampart One is designed to minimize the exposure and vascular retraction requirements associated with traditional anterior spinal fusion procedures. The system includes both standard and oblique interbody device footprints each with integrated fixation screws.

CEO of Spineology John Booth explains: “Minimizing exposure and retraction are cornerstone elements of all Spineology anatomy conserving designs. We are very excited about this approval and look forward to entering the anterior market in the near future.”

Dr. Jeremy Shore of Boston, Massachusetts added, “Variable angle instrumentation and integrated guides are colinear with the access, providing the surgeon the ability to keep the incision to a minimum,”

“For instances where there is limited to no vessel mobility, the Rampart One Oblique footprint is an excellent option,” adds Dr. Clifford Tribus of Madison, Wisconsin.

Rampart One is manufactured from Invibio® PEEK-OPTIMA® HA Enhanced material. This provides an improved osteoconductive surface for bone on-growth while preserving the traditional benefits of PEEK-OPTIMA Natural including a modulus similar to bone, reduced stress shielding and artifact-free imaging.

Medical Device News Magazinehttps://infomeddnews.com
Medical Device News Magazine is a division of PTM Healthcare Marketing, Inc. Pauline T. Mayer is the managing editor.

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