ulrich Medical USA receives FDA 510(k) clearance of 3D-printed cervical interbody device

Fact checked byGina Brockenbrough, MA

ulrich Medical USA Inc. has announced FDA 510(k) clearance of the Flux-C, a 3D-printed porous titanium cervical interbody device, according to a company press release.

The porous titanium component of the Flux-C device is designed with large graft windows to allow for improved radiographic imaging, according to the release.

The main entrance of FDA Building 1. — Flux-C is a 3D-printed porous titanium cervical interbody device, Source: Adobe Stock

“We are continuing to develop procedural solutions for reconstruction of all spinal pathologies in collaboration with our surgeon advisory board,” Eric Lucas, PhD, director of technology for ulrich Medical USA, said in the release. “We strive to help our surgeons and distributors achieve new heights and beyond with integrity, through excellence in design, manufacturing and craftsmanship,” Lucas said.

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ulrich Medical USA receives FDA 510(k) clearance of 3D-printed cervical interbody device

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