FDA PMA
FDA Class 3
Approved
🇺🇸 United States
Replacement Heart-Valve
PMA: P990064
·
Supplement: S006
·
Decision Jan 18, 2002
Classifications
1
FEI Numbers
11
Registration Numbers
11
Basic Information
- Device Name
- Replacement Heart-Valve
- Trade Name
- MOSAIC PORCINE BIOPROSTHESIS
- PMA Number
- P990064
- Supplement Number
- S006
- Device Class
- FDA Class 3
- Product Code
- DYE
- Generic Name
- replacement Heart-valve
- Regulation Number
- 870.3925
- Medical Specialty
- Cardiovascular
- Advisory Committee
- Cardiovascular
- Decision
- Approved
- Decision Code
- APPR
- Decision Date
- January 18, 2002
- Date Received
- July 26, 2001
- Supplement Type
- Normal 180 Day Track
- Supplement Reason
- Change Design/Components/Specifications/Material
- Expedited Review
- N
Advisory Committee Statement
APPROVAL FOR THE MOSAIC PORCINE BIOPROSTHESIS, MODEL 305 AORTIC, 19MM.
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 |
|---|---|---|---|
| DYE | Replacement Heart-Valve | FDA class 3 | Cardiovascular |