FDA PMA
FDA Class 3
Approved
🇺🇸 United States
Sealant, Polymerizing
PMA: P030039
·
Supplement: S013
·
Decision Sep 3, 2009
Classifications
1
FEI Numbers
15
Registration Numbers
15
Basic Information
- Device Name
- Sealant, Polymerizing
- Trade Name
- COSEAL SURGICAL SEALANT DEVICE
- PMA Number
- P030039
- Supplement Number
- S013
- Device Class
- FDA Class 3
- Product Code
- NBE
- Generic Name
- Sealant, polymerizing
- Medical Specialty
- Unknown
- Advisory Committee
- General, Plastic Surgery
- Decision
- Approved
- Decision Code
- APPR
- Decision Date
- September 3, 2009
- Date Received
- March 17, 2009
- 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 NEW SUPPLIER OF PEG COMPONENT MATERIAL.
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 |
|---|---|---|---|
| NBE | Sealant, Polymerizing | FDA class 3 | Unknown |