PMA supplement
P180002 S019: Zephyr Endobronchial Valve (Zephyr Valve)
FDA PMA supplement · Normal 180 Day Track No User Fee · Pulmonx Corporation
Key facts
| Original PMA | P180002 |
|---|---|
| Supplement number | S019 |
| Supplement type | Normal 180 Day Track No User Fee |
| Reason for the supplement | Postapproval Study Protocol |
| Trade name | Zephyr Endobronchial Valve (Zephyr Valve) |
| Generic name | Valve, pulmonary |
| Applicant | Pulmonx Corporation |
| Product code | NJK |
| Received date | Jul 16, 2021 |
| Decision date | Aug 13, 2021 |
At a glance
- No Expedited review granted
- No Approval order on file
- No Summary of safety and effectiveness on file
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About PMA supplements
A PMA supplement asks FDA to approve a change to a device that already holds a premarket approval: a new indication, a design or labeling change, a manufacturing site or process change.
Source: U.S. Food and Drug Administration (FDA), Premarket Approval (PMA) database · Source date: