PMA supplement
P200028 S014: DIAMOND AF
FDA PMA supplement · Normal 180 Day Track No User Fee · Medtronic, Inc.
Key facts
| Original PMA | P200028 |
|---|---|
| Supplement number | S014 |
| Supplement type | Normal 180 Day Track No User Fee |
| Reason for the supplement | Postapproval Study Protocol |
| Trade name | DIAMOND AF |
| Generic name | Catheter, percutaneous, cardiac ablation, for treatment of atrial fibrillation |
| Applicant | Medtronic, Inc. |
| Product code | OAE |
| Received date | Oct 17, 2022 |
| Decision date | Nov 16, 2022 |
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: