FDA PMA
FDA Class 3
Approved
🇺🇸 United States
Agent, Bulking, Injectable For Gastro-Urology Use
PMA: P100014
·
Supplement: S004
·
Decision Oct 27, 2011
Classifications
1
FEI Numbers
16
Registration Numbers
16
Basic Information
- Device Name
- Agent, Bulking, Injectable For Gastro-Urology Use
- Trade Name
- SOLESTA
- PMA Number
- P100014
- Supplement Number
- S004
- 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
- October 27, 2011
- Date Received
- October 13, 2011
- Supplement Type
- Normal 180 Day Track No User Fee
- Supplement Reason
- Postapproval Study Protocol - OSB
- Expedited Review
- N
Advisory Committee Statement
APPROVAL OF THE POST-APPROVAL PROTOCOL.
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 |