FDA PMA
FDA Class 3
30-Day Notice Accepted
🇺🇸 United States
Heart-Valve, Mechanical
PMA: P790018
·
Supplement: S044
·
Decision Sep 23, 2003
Classifications
1
FEI Numbers
17
Registration Numbers
17
Basic Information
- Device Name
- Heart-Valve, Mechanical
- Trade Name
- MEDTRONIC HALL PROSTHETIC HEART VALVES (MODELS A7700 AND M7700)
- PMA Number
- P790018
- Supplement Number
- S044
- Device Class
- FDA Class 3
- Product Code
- LWQ
- Generic Name
- HEART-VALVE, MECHANICAL
- Medical Specialty
- Unknown
- Advisory Committee
- Cardiovascular
- Decision
- 30-Day Notice Accepted
- Decision Code
- OK30
- Decision Date
- September 23, 2003
- Date Received
- August 29, 2003
- Supplement Type
- 30-Day Notice
- Supplement Reason
- Process Change - Manufacturer/Sterilizer/Packager/Supplier
- Expedited Review
- N
Advisory Committee Statement
ELIMINATION OF THE PRODUCTION PULSE DUPLICATION TEST FROM THE MANUFACTURING PROCESS.
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 |