Spineart, a company specializing in rapid growth in spine surgery, proudly announces the FDA's 510(k) clearance for its SCARLET® AC-Ti anterior cervical cage.

Building on a decade of experience with the SCARLET® system, SCARLET® AC-Ti introduces new features like the MIMETIX® morphometric profile.

This profile, developed using digital vertebrae models, optimizes the contact surface between the implant and vertebral endplates. The system allows fixation with screws and anchors.

Utilizing Spineart's patented Ti-LIFE technology, the SCARLET® AC-Ti cervical cage boasts a porous structure that mimics trabecular bone.

"This clearance underscores our commitment to innovation and the ongoing evolution of our most successful products, like the SCARLET® system," explained, Spineart's Commercial Director.







Source: prnewswire.com

 

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