the four criteria for program eligibility that CMS had previously proposed. The TCET pathway will facilitate coverage only for devices that have Breakthrough designation from the FDA, are ...

Manufacturers of FDA-designated breakthrough devices that ... is generated to support a long-term NCD. Guidance for Developers of Medical Devices for Treatment of Opioid Use Disorder In 2018 ...

The system consists of an endovascularly implantable CSF shunt and delivery components for bypass invasive surgery.

Though the U.S. continues to lead the world as a life science capital, outspending every country on earth in research and ...

Public Forum 2024 kicked off this week with experts from the National Evaluation System for health Technology (NEST), the ...

The many industry partnerships across UCSF include: Facebook: UCSF was among the first universities to join an innovative development model sponsored by Facebook’s Building 8, a venture that “applies ...

Sonic Incytes Medical Corp, a leader in point-of-care ultrasound, proudly announces that the U.S. Food and Drug Administration (FDA) has granted 510(k) clearance for its Velacur® Determined Fat ...

The medical device/technology subsectors lagged on concerns that pent-up demand from COVID-19 could wane in the second half of 2024. Some firms also lowered sales guidance ... accelerated approval for ...