FDA PMA
FDA Class 3
30-Day Notice Accepted
🇺🇸 United States
Agent, Bulking, Injectable For Gastro-Urology Use
PMA: P980053
·
Supplement: S015
·
Decision Aug 19, 2013
Classifications
1
FEI Numbers
16
Registration Numbers
16
Basic Information
- Device Name
- Agent, Bulking, Injectable For Gastro-Urology Use
- Trade Name
- DURASPHERE INJECTABLE BULKING AGENT
- PMA Number
- P980053
- Supplement Number
- S015
- 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
- August 19, 2013
- Date Received
- July 22, 2013
- Supplement Type
- 30-Day Notice
- Expedited Review
- N
Advisory Committee Statement
ADDITION OF A NEW TEXTURE ANALYZER SYSTEM.
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 |