PMA
P980033: WALLSTENT ENDOPROSTHESIS
FDA PMA · Stent, central venous · Boston Scientific Corporation
Key facts
| PMA number | P980033 |
|---|---|
| Trade name | WALLSTENT ENDOPROSTHESIS |
| Generic name | Stent, central venous |
| Applicant | Boston Scientific Corporation |
| Owner/operator | Boston Scientific Corporation |
| Product code | QKJ |
| Approval date | Nov 16, 2001 |
| Docket number | 02M-0203 |
| Notice date | May 9, 2002 |
| Establishment registration | 2134265 |
| FEI number | 3002095335 |
At a glance
- 10–99 Supplements
- May 6, 2026 Latest supplement decision
- No Withdrawn
- Yes Summary of safety and effectiveness on file
- 10–99 UDI device identifiers (GUDID)
- None MAUDE adverse event reports
- None Recall events
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About PMA approvals
Premarket approval (PMA) is the FDA's most stringent review pathway, required for most Class III devices that support or sustain life or present a potentially unreasonable risk.
Source: U.S. Food and Drug Administration (FDA), Premarket Approval (PMA) database · Source date: