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

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.

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