PMA supplement
P150005 S043: Maestro™ Ablation Connection Box, IntellaNav™ XP and IntellaNav™ MiFi XP
FDA PMA supplement · Real-Time Process · Boston Scientific Corp
Key facts
| Original PMA | P150005 |
|---|---|
| Supplement number | S043 |
| Supplement type | Real-Time Process |
| Reason for the supplement | Change Design/Components/Specifications/Material |
| Trade name | Maestro™ Ablation Connection Box, IntellaNav™ XP and IntellaNav™ MiFi XP |
| Generic name | Catheter, percutaneous, cardiac ablation, for treatment of atrial flutter |
| Applicant | Boston Scientific Corp |
| Product code | OAD |
| Received date | Mar 22, 2019 |
| Decision date | May 29, 2019 |
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: