FDA PMA
FDA Class 3
Approved
🇺🇸 United States
Ventricular (Assist) Bypass
PMA: P900023
·
Supplement: S047
·
Decision Dec 11, 2007
Classifications
1
FEI Numbers
21
Registration Numbers
21
Basic Information
- Device Name
- Ventricular (Assist) Bypass
- Trade Name
- IPULSE CIRCULATORY SUPPORT SYSTEM
- PMA Number
- P900023
- Supplement Number
- S047
- Device Class
- FDA Class 3
- Product Code
- DSQ
- Generic Name
- Ventricular (assist) bypass
- Medical Specialty
- Unknown
- Advisory Committee
- Cardiovascular
- Decision
- Approved
- Decision Code
- APPR
- Decision Date
- December 11, 2007
- Date Received
- November 13, 2006
- Supplement Type
- Normal 180 Day Track
- Supplement Reason
- Change Design/Components/Specifications/Material
- Expedited Review
- N
Advisory Committee Statement
APPROVAL FOR THE IPULSE CIRCULATORY SUPPORT SYSTEM, A UNIT THAT WILL SUPPORT PATIENTS IN NEED OF FULL CIRCULATORY SUPPORT USING THE BVS 5000 BLOOD PUMP OR THE AB5000 VENTRICLE, OR PARTIAL VENTRICULAR ASSIST USING THE APPROVED INTRA-AORTIC BALLOON PUMP (IABP). THE DEVICE CONSOLE, AS MODIFIED, WILL BE MARKETED UNDER THE TRADE NAME IPULSE CIRCULATORY SUPPORT SYSTEM AND IS INDICATED FOR USE IN CONJUNCTION WITH THE ABIOMED AB 5000 VENTRICLE AND THE BVS 5000 BLOOD PUMP.
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 |
|---|---|---|---|
| DSQ | Ventricular (Assist) Bypass | FDA class 3 | Unknown |