PMA supplement
P020025 S015: EP TECH EPT-1000XP RF ABLATION SYSTEM
FDA PMA supplement · Normal 180 Day Track No User Fee · Boston Scientific
Key facts
| Original PMA | P020025 |
|---|---|
| Supplement number | S015 |
| Supplement type | Normal 180 Day Track No User Fee |
| Reason for the supplement | Express GMP Supplement |
| Trade name | EP TECH EPT-1000XP RF ABLATION SYSTEM |
| Generic name | Cardiac ablation percutaneous catheter |
| Applicant | Boston Scientific |
| Product code | LPB |
| Received date | Oct 13, 2005 |
| Decision date | Jul 8, 2009 |
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: