PMA supplement
P860057 S152: Carpentier-Edwards PERIMOUNT Magna Pericardial Aortic Bioprosthesis 3000, with ThermaFix tissue process 3000TFX,Ease Per
FDA PMA supplement · Real-Time Process · Edwards Lifesciences, LLC
Key facts
| Original PMA | P860057 |
|---|---|
| Supplement number | S152 |
| Supplement type | Real-Time Process |
| Reason for the supplement | Labeling Change - Indications/instructions/shelf life/tradename |
| Trade name | Carpentier-Edwards PERIMOUNT Magna Pericardial Aortic Bioprosthesis 3000, with ThermaFix tissue process 3000TFX,Ease Per |
| Generic name | Replacement Heart-valve |
| Applicant | Edwards Lifesciences, LLC |
| Product code | DYE |
| Received date | Aug 12, 2016 |
| Decision date | Oct 20, 2016 |
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: