FDA PMA
FDA Class 3
Approved
🇺🇸 United States
Heart-Valve, Mechanical
PMA: P830039
·
Supplement: S010
·
Decision Oct 29, 1999
Classifications
1
FEI Numbers
17
Registration Numbers
17
Basic Information
- Device Name
- Heart-Valve, Mechanical
- Trade Name
- OMNISCIENCE CARDIAC VALVE
- PMA Number
- P830039
- Supplement Number
- S010
- Device Class
- FDA Class 3
- Product Code
- LWQ
- Generic Name
- HEART-VALVE, MECHANICAL
- Medical Specialty
- Unknown
- Advisory Committee
- Cardiovascular
- Decision
- Approved
- Decision Code
- APPR
- Decision Date
- October 29, 1999
- Date Received
- May 4, 1999
- Supplement Type
- Normal 180 Day Track
- Supplement Reason
- Labeling Change - Indications/instructions/shelf life/tradename
- Expedited Review
- N
Advisory Committee Statement
Approval for modifications to the Omni-Series Instructions for Handling and Use.
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 |
|---|---|---|---|
| LWQ | Heart-Valve, Mechanical | FDA class 3 | Unknown |