Cervical Stalif C Ti

Raising the Gold Standard with The Ti-ACTIVE surface provides a three-dimensional texturized surface that is microporous with hydrophilic properties, to facilitate human mesenchymal stem cell (hMSC) attachment and proliferation as demonstrated by pre-clinical testing performed on representative PEEK coupons with Ti-ACTIVE surface.

During manufacturing, commercially pure titanium (CP Ti) is applied to the PEEK cage by a plasma spray to create our Ti-ACTIVE devices. The unique CP Ti surface system utilizes a robotic applicator, enabling the creation of a high-quality, reproducible titanium surface. Ti-ACTIVE was tested for mechanical integrity and the results exceeded the FDA requirements for shear and tensile strength for metallic spray surfaces.  

The STALIF C-Ti device is engineered to achieve equivalent biomechanical performance to anterior plate & cage technologies.

STALIF C screws provide an added layer of security with an Anti Back-Out (ABO) titanium split-ring which first compresses and then deploys during insertion.  

No-Profile; No Supplemental Fixation. STALIF C's integrated cage and screw system is cleared for use without supplemental fixation, while the "No-Profile" design allows it to nest fully within the confines of the vertebral body—leaving the anatomy unchanged external to the interbody.

Compressive lag fixation ensures biomechanical stability and provides secure graft-endplate contact. Lag screws reduce the vertebral bodies onto the PEEK Cage creating graft / endplate surface compression to provide the best opportunity for fusion.