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Clinical Literature

Since 2008, the Spiration® Valve System has been approved by the FDA as a Humanitarian Use Device for the control of prolonged air leaks following specified lung resections.*


CLICK HERE to find a library of current articles, abstracts, and white papers regarding bronchial valve treatment for air leaks. 

 

Physician Education


The FDA has approved the Spiration Valve System under the Humanitarian Use Device label. Under this approval, a physician at each site must complete a thorough training course before the site is approved for commercial use. Spiration has developed a state-of-the-art physician training program designed to provide the physician with the knowledge and practical experience to treat air leak patients with the Spiration Valve System.

Training will cover physician and hospital requirements for working with a Humanitarian Use Device.

To request training and/or site qualification please complete the Contact form.