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An internationally advanced cervical non-fusion product intended for single/two-level symptomatic cervical disc replacement at C3-C7.
It preserves cervical motion and reduces the risk of adjacent segment degeneration. Single-level surgery takes approximately 40 minutes. The product has been used in more than 60 countries worldwide with over 70,000 implantations, and has demonstrated excellent outcomes in 10-year clinical follow-up.
Guided mobile nucleus
The guided mobile PE nucleus design avoids excessive constraint on the facet joints and allows 6 degrees of motion.
Anatomical design
The wedge-shaped curved anatomical design maximizes the fit of the artificial disc to the intervertebral space and optimizes coverage of the vertebral endplates.
Reduced MRI artifacts
Titanium endplates are coated with diamond-like carbon (DLC), minimizing MRI artifacts and enabling more comprehensive postoperative follow-up for patients.
Radiolucent inserter
The radiolucent inserter allows verification of the anterior positioning and accurate implantation of the device. Its design enables pre-assembly of the prosthesis for improved surgical handling.