PMA supplement
P020014 S008: ESSURE SYSTEM
FDA PMA supplement · Real-Time Process · Bayer Pharma AG
Key facts
| Original PMA | P020014 |
|---|---|
| Supplement number | S008 |
| Supplement type | Real-Time Process |
| Reason for the supplement | Process Change - Manufacturer/Sterilizer/Packager/Supplier |
| Trade name | ESSURE SYSTEM |
| Generic name | Transcervical contraceptive tubal occlusion device |
| Applicant | Bayer Pharma AG |
| Product code | HHS |
| Received date | Sep 20, 2004 |
| Decision date | Jan 31, 2005 |
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: