The Tritanium PL Posterior Lumbar Cage is an intervertebral body fusion device that aids in lumbar spinal fixation for patients with degenerative disc disease, has received 510(k) clearance from the U.S. Food and Drug Administration. The Tritanium PL posterior lumbar cages are constructed out of proprietary Tritanium technology and are manufactured via a 3D additive manufacturing process.
Tritanium is a novel highly porous titanium material designed for bone in-growth and biologic fixation in spine applications. Tritanium PL Cages are offered in a variety of widths, lengths, heights, and lordotic angles designed to adapt to a variety of patient anatomies and are designed to be implanted via a posterior approach.
The large lateral windows and open architecture of the Tritanium PL Cage allow visualization of fusion on CT and X-ray. Its solid-tipped, precisely angled serrations are designed for bidirectional fixation and to maximize surface area for endplate contact with the implant. The Tritanium PL Cage is also designed to address the potential for subsidence into the endplates.
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