Konica Minolta’s dynamic digital x-ray gains FDA clearance
The FDA has granted Konica Minolta Healthcare Americas 510(k) clearance for its dynamic digital radiography (DDR) imaging system.
The x-ray technology can depict movement and allows radiologists to annotate images for a more detailed clinical finding, according to the company. DDR also enables clinicians to observe the dynamic interaction of anatomical structures such as tissue and bone over time.
Konica Minolta believes their DDR system can have the strongest impact in musculoskeletal (MSK) and thoracic imaging. For example, orthopedists commonly rely on external motion and static x-ray to evaluate joint stability and spinal movement; with DDR, specialists can look at a full view of the MSK system in multiple positions to analyze bone changes throughout the entire range of motion.
“DDR is a paradigm shift in how x-ray may be utilized throughout the continuum of care, where an essential primary diagnostic tool can now deliver more information so clinicians can visualize anatomic structures and their interaction during movement in a way they have never seen before,” said Guillermo Sander, director of digital radiography marketing, Konica Minolta Healthcare, in a prepared statement. “There are immense opportunities for DDR to help clinicians enhance patient management and personalize care with potential cost savings by reducing the need for more advanced and expensive imaging tests.”