PMA supplement
P220013 S015: TactiFlex Ablation Catheter, Sensor Enabled (TactiFlex SE)
FDA PMA supplement · 30-Day Notice · ABBOTT MEDICAL
Key facts
| Original PMA | P220013 |
|---|---|
| Supplement number | S015 |
| Supplement type | 30-Day Notice |
| Reason for the supplement | Process Change - Manufacturer/Sterilizer/Packager/Supplier |
| Trade name | TactiFlex Ablation Catheter, Sensor Enabled (TactiFlex SE) |
| Generic name | Catheter, percutaneous, cardiac ablation, for treatment of atrial fibrillation |
| Applicant | ABBOTT MEDICAL |
| Product code | OAE |
| Received date | Oct 30, 2024 |
| Decision date | Nov 27, 2024 |
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: