@ShahidNShah
A global leader in interventional pulmonology, planning tools, and treatments for obstructive lung disease. Based in Redwood City, California, and Neuchâtel, Switzerland, Pulmonx is the maker of the Zephyr Endobronchial Valve. The Zephyr® Valve was granted breakthrough status and approved by the FDA in June 2018, because according to the FDA it “represents a breakthrough technology as the device offers bronchoscopic lung volume reduction without surgery and its associated risks. This device offers a significant, clinically meaningful advantage over the current standard of care and therefore, its availability is also in the best interest of patients.”
Zephyr Valves are proven to help emphysema patients breathe easier, be more active, and enjoy a better quality of life. The Zephyr Endobronchial Valve is an FDA-approved device for patients with …
Posted General Care Management FDA Breakthrough Device Designation
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