FDA OKs 3D mode for Biospace Med's EOS

AuntMinnieEurope.com staff writers

Oct 7, 2008

French digital radiography developer Biospace Med of Paris has received 510(k) clearance from the U.S. Food and Drug Administration (FDA) for a 3D skeletal reconstruction mode for its EOS digital x-ray system.

sterEOS is designed to enable EOS to perform 3D skeletal reconstructions for applications such as visualizing spine pathologies and hip and knee arthropathies. The EOS system captures head-to-toe images of patients in a standing, weight-bearing position at reduced radiation dose. The system received FDA clearance in 2007.

sterEOS includes a 3D visualization workstation and is designed to reduce surgical planning time and help establish an effective course of treatment.

Related Reading

Biospace adds Latin American distributor, November 30, 2007

Biospace raises $18 million, November 27, 2007

Biospace adds to executive lineup, November 19, 2007

Road to RSNA, Digital X-Ray, Biospace Med, October 23, 2007

Biospace Med nets FDA OK on x-ray imager, October 9, 2007

Copyright © 2008 AuntMinnie.com

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