December 4, 2022
1 minute Read
According to a company press release, ulrich Medical USA Inc. has granted FDA 510(k), approval for Flux-C. This is a 3D-printed porous-titanium cervical interbody device.
Flux-C’s porous titanium device has large graft window to enable radiographic imaging to be improved, according to the release.
“We are continuing to develop procedural solutions for reconstruction of all spinal pathologies in collaboration with our surgeon advisory board,” Eric Lucas, PhD The release stated that ulrich Medical USA’s director of technology was the spokesperson. “We strive to help our surgeons and distributors achieve new heights and beyond with integrity, through excellence in design, manufacturing and craftsmanship,” Lucas said.