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Home » Spineart wins FDA clearance for Scarlet AC-Ti anterior cervical cage

Spineart wins FDA clearance for Scarlet AC-Ti anterior cervical cage

May 30, 2024 By Danielle Kirsh

Scarlet AC-Ti product image.
[Image courtesy of Spineart]
Spineart recently announced it received FDA 510(k) clearance for its Scarlet AC-Ti secured anterior cervical cage.

Scarlet AC-Ti uses a Mimetix morphometric profile developed with digital vertebrae models to optimize the contact surface between the implant and endplates. The entire system allows for fixation with screws and anchors.

“This approval underscores our commitment to innovation, continuously evolving our most successful products, such as the Scarlet system,” Chief Commercial Officer Alessia Erlingher said in a news release.

The Scarlet AC-Ti cervical cage also uses Spineart’s Ti-Life technology, a proprietary additive manufacturing process. Its porous structure closely mimics that of trabecular bone.

Spineart’s latest Scarlet AC-Ti builds upon more than a decade of development for the Scarlet spinal device line. The company has a few devices under the Scarlet umbrella, including the Scarlet AL-T secured lumbar anterior cage and the Scarlet AC-T secured cervical cage.

Filed Under: Orthopedics, Spine Tagged With: Spineart

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About Danielle Kirsh

Danielle Kirsh is an award-winning journalist and senior editor for Medical Design & Outsourcing, MassDevice, and Medical Tubing + Extrusion, and the founder of Women in Medtech and lead editor for Big 100. She received her bachelor's degree in broadcast journalism and mass communication from Norfolk State University and is pursuing her master's in global strategic communications at the University of Florida. You can connect with her on Twitter and LinkedIn, or email her at [email protected].

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