FDA PMA
FDA Class 3
Approved
🇺🇸 United States
Agent, Absorbable Hemostatic, Non-Collagen Based
PMA: P050038
·
Supplement: S042
·
Decision Nov 4, 2024
Classifications
1
FEI Numbers
29
Registration Numbers
29
Basic Information
- Device Name
- Agent, Absorbable Hemostatic, Non-Collagen Based
- Trade Name
- Arista AH
- PMA Number
- P050038
- Supplement Number
- S042
- Device Class
- FDA Class 3
- Product Code
- LMG
- Generic Name
- Agent, absorbable hemostatic, non-collagen based
- Regulation Number
- 878.4490
- Medical Specialty
- General, Plastic Surgery
- Advisory Committee
- General, Plastic Surgery
- Decision
- Approved
- Decision Code
- APPR
- Decision Date
- November 4, 2024
- Date Received
- May 3, 2024
- Supplement Type
- 135 Review Track For 30-Day Notice
- Supplement Reason
- Process Change - Manufacturer/Sterilizer/Packager/Supplier
- Expedited Review
- N
Advisory Committee Statement
change in the raw material potato starch in the manufacturing of Arista AH
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 |
|---|---|---|---|
| LMG | Agent, Absorbable Hemostatic, Non-Collagen Based | FDA class 3 | General, Plastic Surgery |