PMA supplement
P900052 S014: PORT-A-CATH EPIDURAL & PORT-A-CATH II LOW PROFILE EPIDURAL SYSTEMS
FDA PMA supplement · 135 Review Track For 30-Day Notice · Smiths Medical Asd, Inc.
Key facts
| Original PMA | P900052 |
|---|---|
| Supplement number | S014 |
| Supplement type | 135 Review Track For 30-Day Notice |
| Reason for the supplement | Process Change - Manufacturer/Sterilizer/Packager/Supplier |
| Trade name | PORT-A-CATH EPIDURAL & PORT-A-CATH II LOW PROFILE EPIDURAL SYSTEMS |
| Generic name | CATHETER, PERCUTANEOUS, LONG TERM, INTRASPINAL |
| Applicant | Smiths Medical Asd, Inc. |
| Product code | LNY |
| Received date | Dec 8, 2006 |
| Decision date | Aug 28, 2007 |
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: