Elixir Medical Granted FDA Breakthrough Device Designation for DynamX Bioadaptor
DAIC
JUNE 18, 2024
FDA Breakthrough Device Designation accelerates the review process for novel technologies that may provide more effective treatment or diagnosis of life-threatening or irreversibly debilitating diseases or conditions, such as CAD, which impacts 7.8% Stent Related Adverse Events greater than 1 Year After PCI. of the U.S. population.
Let's personalize your content