FDA PMA
FDA Class 3
30-Day Notice Accepted
🇺🇸 United States
Agent, Bulking, Injectable For Gastro-Urology Use
PMA: P040050
·
Supplement: S005
·
Decision Jul 2, 2010
Classifications
1
FEI Numbers
16
Registration Numbers
16
Basic Information
- Device Name
- Agent, Bulking, Injectable For Gastro-Urology Use
- Trade Name
- MACROPLASTIQUE IMPLANTS
- PMA Number
- P040050
- Supplement Number
- S005
- Device Class
- FDA Class 3
- Product Code
- LNM
- Generic Name
- AGENT, BULKING, INJECTABLE FOR GASTRO-UROLOGY USE
- Medical Specialty
- Unknown
- Advisory Committee
- Gastroenterology, Urology
- Decision
- 30-Day Notice Accepted
- Decision Code
- OK30
- Decision Date
- July 2, 2010
- Date Received
- June 3, 2010
- Supplement Type
- 30-Day Notice
- Supplement Reason
- Process Change - Manufacturer/Sterilizer/Packager/Supplier
- Expedited Review
- N
Advisory Committee Statement
ALTERNATE VENDOR FOR THE INNER AND OUTER MACROPLASTIQUE IMPLANTS PACKAGING.
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 |
|---|---|---|---|
| LNM | Agent, Bulking, Injectable For Gastro-Urology Use | FDA class 3 | Unknown |