FDA PMA
FDA Class 3
Approved
🇺🇸 United States
Drug-Coated Peripheral Transluminal Angioplasty Catheter
PMA: P190008
·
Supplement: S004
·
Decision Sep 24, 2020
Classifications
1
FEI Numbers
7
Registration Numbers
7
Basic Information
- Device Name
- Drug-Coated Peripheral Transluminal Angioplasty Catheter
- Trade Name
- IN.PACT AV Paclitaxel-coated Percutaneous Transluminal Angioplasty (PTA) Balloon Catheter
- PMA Number
- P190008
- Supplement Number
- S004
- Device Class
- FDA Class 3
- Product Code
- PRC
- Generic Name
- Drug-coated peripheral transluminal angioplasty catheter
- Medical Specialty
- Unknown
- Advisory Committee
- Cardiovascular
- Decision
- Approved
- Decision Code
- APPR
- Decision Date
- September 24, 2020
- Date Received
- June 26, 2020
- Supplement Type
- Real-Time Process
- Supplement Reason
- Change Design/Components/Specifications/Material
- Expedited Review
- N
Advisory Committee Statement
Approval for a packaging change to the shelf carton.
Classifications
This FDA Pre-Market Approval entry is associated with 1 FDA classification via its product code.
| Product Code | Device Name | Device Class | Medical Specialty |
|---|---|---|---|
| PRC | Drug-Coated Peripheral Transluminal Angioplasty Catheter | FDA class 3 | Unknown |