FDAnews Device Daily Bulletin
Medical Devices / Submissions and Approvals

Stryker Receives FDA Clearance for 3D-Printed Tritanium C Anterior Cervical Cage

Sept. 25, 2017
A A

Stryker’s received 510(k) clearance for its Tritanium C anterior cervical cage, a 3D printer interbody fusion cage for use in the cervical spine.

The device is constructed from Stryker’s proprietary Tritanium In-Growth Technology, a porous titanium material designed for bone in-growth and biological fixation. The device features an open central graft window and lateral windows to help reduce stiffness of the cage and minimize subsidence.

The device is indicated for use in cervical interbody fusion procedures in skeletally mature patients with degenerative disc disease.

View today's stories