FDA PMA
FDA Class 3
Approved
🇺🇸 United States
Heart-Valve, Mechanical
PMA: P810002
·
Supplement: S084
·
Decision Aug 19, 2013
Classifications
1
FEI Numbers
17
Registration Numbers
17
Basic Information
- Device Name
- Heart-Valve, Mechanical
- Trade Name
- REGENT MECHANICAL HEART VALVE
- PMA Number
- P810002
- Supplement Number
- S084
- 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
- August 19, 2013
- Date Received
- April 4, 2013
- Supplement Type
- 135 Review Track For 30-Day Notice
- Supplement Reason
- Process Change - Manufacturer/Sterilizer/Packager/Supplier
- Expedited Review
- N
Advisory Committee Statement
APPROVAL FOR A CHANGE TO THE INSPECTION SAMPLING PLAN FOR FINAL LEAFLET EAR THICKNESS DIMENSIONS.
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 |