PMA supplement
P020014 S051: Essure System for Permanent Birth Control
FDA PMA supplement · Special (Immediate Track) · Bayer Pharma AG
Key facts
| Original PMA | P020014 |
|---|---|
| Supplement number | S051 |
| Supplement type | Special (Immediate Track) |
| Reason for the supplement | Labeling Change - Indications/instructions/shelf life/tradename |
| Trade name | Essure System for Permanent Birth Control |
| Generic name | Transcervical contraceptive tubal occlusion device |
| Applicant | Bayer Pharma AG |
| Product code | HHS |
| Received date | Apr 4, 2018 |
| Decision date | Apr 9, 2018 |
At a glance
- No Expedited review granted
- Yes 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: