FDA PMA
FDA Class 3
30-Day Notice Accepted
🇺🇸 United States
Barrier, Absorbable, Adhesion
PMA: P950034
·
Supplement: S025
·
Decision May 28, 2003
Classifications
1
FEI Numbers
17
Registration Numbers
17
Basic Information
- Device Name
- Barrier, Absorbable, Adhesion
- Trade Name
- SEPRAFILM ADHESION BARRIER/SEPRAFILM PROCEDURE PACK
- PMA Number
- P950034
- Supplement Number
- S025
- Device Class
- FDA Class 3
- Product Code
- MCN
- Generic Name
- Barrier, absorbable, adhesion
- Medical Specialty
- Unknown
- Advisory Committee
- General, Plastic Surgery
- Decision
- 30-Day Notice Accepted
- Decision Code
- OK30
- Decision Date
- May 28, 2003
- Date Received
- April 30, 2003
- Supplement Type
- 30-Day Notice
- Supplement Reason
- Process Change - Manufacturer/Sterilizer/Packager/Supplier
- Expedited Review
- N
Advisory Committee Statement
MANUFACTURING PROCESS CHANGE TO EXTEND THE ENDOTOXIN SPECIFICATION LIMIT OF HYALURONIC ACID (HA) RAW MATERIAL FROM <=0.04 EU/MG TO <=0.08 EU/MG.
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 |
|---|---|---|---|
| MCN | Barrier, Absorbable, Adhesion | FDA class 3 | Unknown |