FDA PMA
FDA Class 3
30-Day Notice Accepted
🇺🇸 United States
Replacement Heart-Valve
PMA: P870077
·
Supplement: S059
·
Decision Mar 14, 2014
Classifications
1
FEI Numbers
11
Registration Numbers
11
Basic Information
- Device Name
- Replacement Heart-Valve
- Trade Name
- DURAFLEX LOW PRESSURE PORCINE MITRAL BIOPROSTHESIS, DURAFLEX LOW PRESSURE MITRAL BIOPROSTHESIS WITH EXTENDED SUTURE
- PMA Number
- P870077
- Supplement Number
- S059
- Device Class
- FDA Class 3
- Product Code
- DYE
- Generic Name
- replacement Heart-valve
- Regulation Number
- 870.3925
- Medical Specialty
- Cardiovascular
- Advisory Committee
- Cardiovascular
- Decision
- 30-Day Notice Accepted
- Decision Code
- OK30
- Decision Date
- March 14, 2014
- Date Received
- February 25, 2014
- Supplement Type
- 30-Day Notice
- Expedited Review
- N
Advisory Committee Statement
CHANGE IN THE POLYESTER CLOTH MANUFACTURING AID.
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 |