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- Mammography
Giotto to Demo Newly Cleared Mammo Systems
Giotto USA will be demonstrating at RSNA 2011 its 3D and 3DL digital mammography systems, which recently received FDA 510(k) clearance.
Giotto USA will be demonstrating at RSNA 2011 its 3D and 3DL digital mammography systems, which recently received FDA 510(k) clearance.
The Giotto systems include a ring-shaped tilting gantry, which the company said provides for patient-friendly face-to-face positioning and easier positioning for the technologist. The 3D has an 18 x 24 cm bucky, and the 3DL has a 24 x 30 cm bucky.
Other features of the systems include Insight View, Giotto’s new image processing software with the second generation Selenium Detector technology, inclined positioning for better visualization, and the opportunity to add the Biopsy Digit stereotactic biopsy device.
FDA Clears Updated AI Platform for Digital Breast Tomosynthesis
November 12th 2024Employing advanced deep learning convolutional neural networks, ProFound Detection Version 4.0 reportedly offers a 50 percent improvement in detecting cancer in dense breasts in comparison to the previous version of the software.
Is the Kaiser Score More Effective than BI-RADS for Assessing Contrast-Enhanced Mammography and MRI?
October 14th 2024For women with breast-enhanced masses, Kaiser scoring (KS) demonstrated a 20 percent higher AUC than BI-RADS classification for contrast-enhanced mammography (CEM) and was comparable to KS for breast MRI.
FDA Clears New Features in AI-Powered Mammography Software Suite
October 11th 2024Therapixel’s MammoScreen suite has received 510(k) FDA clearances for a breast density assessment feature and updated software that includes automated pre-reporting, which reportedly expedites reporting of mammography findings.
