Criteria
Endobronchial valves that are approved by the United States Food and Drug Administration (U.S. FDA) (i.e., the Spiration Valve System and Zephyr Valve System) may be considered medically necessary for the treatment of adult individuals with hyperinflation related to severe or very severe emphysema in regions of the lung that have little to no collateral ventilation.
Endobronchial valve not meeting the criteria as indicated in this policy is considered experimental/investigational, and therefore, non-covered because the safety and/or effectiveness of this service cannot be established by the available published peer-reviewed literature.
Procedure Codes