FDA PMA
FDA Class 2
Approved
🇺🇸 United States
Graft, Vascular, Synthetic/Biologic Composite
PMA: P890045
·
Supplement: S003
·
Decision Dec 7, 1993
Classifications
1
FEI Numbers
6
Registration Numbers
6
Basic Information
- Device Name
- Graft, Vascular, Synthetic/Biologic Composite
- Trade Name
- VASCUTEK GELSOFT(TM) VASCULAR GRAFT
- PMA Number
- P890045
- Supplement Number
- S003
- Device Class
- FDA Class 2
- Product Code
- MAL
- Generic Name
- GRAFT, VASCULAR, SYNTHETIC/BIOLOGIC COMPOSITE
- Regulation Number
- 870.3450
- Medical Specialty
- Cardiovascular
- Advisory Committee
- Cardiovascular
- Decision
- Approved
- Decision Code
- APPR
- Decision Date
- December 7, 1993
- Date Received
- November 5, 1993
- Supplement Type
- Normal 180 Day Track
- Supplement Reason
- Labeling Change - Indications/instructions/shelf life/tradename
- Expedited Review
- N
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 |
|---|---|---|---|
| MAL | Graft, Vascular, Synthetic/Biologic Composite | FDA class 2 | Cardiovascular |