FDAnews Device Daily Bulletin
Medical Devices / Submissions and Approvals

Stryker’s Tritanium TL Lumbar Cage Gains 510(k) Clearance

March 8, 2018
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Stryker received 510(k) clearance for its Tritanium TL curved posterior lumbar cage, an interbody fusion cage intended for lumbar fixation.

The device is a hollow implant that uses a material designed for bone ingrowth and biological fixation and complements Stryker’s Titanium PL cage. It is shaped for steerability and is designed so the cage can be rotated.

The Tritanium TL is indicated for use with autograft and/or allogenic bone graft comprised of cancellous and/or corticocancellous bone graft.

The product will be available in the second quarter of 2018, Stryker said.

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