FDA PMA
FDA Class 3
Approved
🇺🇸 United States
Agent, Bulking, Injectable For Gastro-Urology Use
PMA: P040050
·
Supplement: S001
·
Decision Jul 27, 2007
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
- S001
- 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
- Approved
- Decision Code
- APPR
- Decision Date
- July 27, 2007
- Date Received
- March 2, 2007
- Supplement Type
- Normal 180 Day Track No User Fee
- Supplement Reason
- Location Change - Manufacturer/Sterilizer/Packager/Supplier
- Expedited Review
- N
Advisory Committee Statement
APPROVAL FOR A MANUFACTURING SITE CHANGE FROM MINNEAPOLIS, MINNESOTA TO MINNETONKA, MINNESOTA.
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 |