Proprio receives FDA clearance of light field-enabled spine surgery navigation platform
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Key takeaways:
- Proprio received FDA 510(k) clearance of its Paradigm spine surgery navigation platform.
- The platform uses light field-enabled technology to show 3D imaging with reduced radiation.
Proprio has announced FDA 510(k) clearance of its Paradigm spine surgery navigation platform, according to a company press release.
The Paradigm platform uses light field technology to show patients’ 3D anatomy with minimized radiation exposure, according to the release.
“We are enthusiastic about the potential for Paradigm to enable clinicians to revolutionize spine surgery,” Gabriel Jones, CEO and co-founder of Proprio, said in the release. “We’re reimagining how surgery is done, rather than reconfiguring legacy tools. This uniquely positions our system to effectively capture the valuable data needed to feed advanced computer vision and deep learning models to recognize, track and analyze complex anatomical structures. The potential of this technology in the hands of skilled clinicians has us all optimistic about the future of surgical practice,” Jones said.
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