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The New CeSpaceXP Cervical Interbody System

June 19, 2013 By Aesculap Implant Systems

Aesculap Implant Systems recently introduced the CeSpaceXP Interbody System for ACDF procedures. The CeSpaceXP fuses two proven materials, an innovative Plasmapore®XP  osteoconductive porous Titanium coating and a PEEK-Optima® radiolucent core, that  delivers enhanced implant stability, artifact-free imaging, and an optimal scaffold for cervical fusion procedures. A comprehensive range of instrument and implant-options are available to accommodate varying patient anatomies and intraoperative needs.

The design advantages of the CeSpaceXP are the result of over 30 years of innovation in spinal technology and over 20 years of success in applying Plasmapore® coatings to Titanium orthopedic and spine implants. Drawing on the success of Plasmapore, Aesculap developed PlasmaporeXP, an osteoconductive porous Titanium coating that can be applied to PEEK spinal implants. PlasmaporeXP is an innovative surface enhancing technology with proven biocompatibility.1

The CeSpaceXP implant brings the market a distinctive interbody design for ACDF procedures. The CeSpaceXP enhances stability and increases migration resistance through the roughened surface area provided by the PlasmaporeXP coating.  The CeSpaceXP offers a comprehensive selection of easy-to-use instrumentation and 30 size options to ensure the best possible fit to patient anatomy and intraoperative flexibility. The CeSpaceXP has excellent imaging properties, incorporating the benefits of the PlasmaporeXP coating, which clearly delineates implant contours during imaging, with X-Ray marker pins for intraoperative positioning and verification.1  

Bob Spiro, PhD, Vice President of Aesculap Biologics and expert in immunology and tissue regeneration said, “The PlasmaporeXP coating found on the CeSpaceXP implant provides the ideal surface composition and architecture for direct bone contact, resulting in higher mechanical strength and improved implant stability.”

The CeSpaceXP is an interbody fusion device designed for use with autogenous bone graft and intended for spinal fusion procedures at one level in the cervical spine from C3 – C7.

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