PMA supplement
P050018 S002: ANGIOSCULPT SCORING BALLOON CATHETER
FDA PMA supplement · Real-Time Process · Spectranetics Corp.
Key facts
| Original PMA | P050018 |
|---|---|
| Supplement number | S002 |
| Supplement type | Real-Time Process |
| Reason for the supplement | Change Design/Components/Specifications/Material |
| Trade name | ANGIOSCULPT SCORING BALLOON CATHETER |
| Generic name | Catheter, percutaneous transluminal coronary angioplasty (ptca), cutting/scoring |
| Applicant | Spectranetics Corp. |
| Product code | NWX |
| Received date | Apr 4, 2007 |
| Decision date | Jul 12, 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: