FDA PMA
FDA Class 3
Approved
🇺🇸 United States
Agent, Bulking, Injectable For Gastro-Urology Use
PMA: P170023
·
Supplement: S003
·
Decision Oct 22, 2020
Classifications
1
FEI Numbers
16
Registration Numbers
16
Basic Information
- Device Name
- Agent, Bulking, Injectable For Gastro-Urology Use
- Trade Name
- Bulkamid Urethral Bulking System
- PMA Number
- P170023
- Supplement Number
- S003
- 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 22, 2020
- Date Received
- August 13, 2020
- Supplement Type
- Real-Time Process
- Supplement Reason
- Change Design/Components/Specifications/Material
- Expedited Review
- N
Advisory Committee Statement
Approval for changes in the primary packaging of Bulkamid Urethral Bulking System (Bulkamid Rotatable Sheath), upgrade to the corresponding process equipment, and replacement of the pouch sealing machine
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 |