FDA PMA
FDA Class 3
30-Day Notice Accepted
🇺🇸 United States
Implanted Fecal Incontinence Device
PMA: P010020
·
Supplement: S003
·
Decision Dec 5, 2006
Classifications
1
FEI Numbers
3
Registration Numbers
3
Basic Information
- Device Name
- Implanted Fecal Incontinence Device
- Trade Name
- ACTICON NEOSPHINCTER ARTIFICIAL BOWEL SPHINCTER
- PMA Number
- P010020
- Supplement Number
- S003
- Device Class
- FDA Class 3
- Product Code
- MIP
- Generic Name
- Implanted fecal incontinence device
- Medical Specialty
- Unknown
- Advisory Committee
- Gastroenterology, Urology
- Decision
- 30-Day Notice Accepted
- Decision Code
- OK30
- Decision Date
- December 5, 2006
- Date Received
- November 6, 2006
- Supplement Type
- 30-Day Notice
- Supplement Reason
- Process Change - Manufacturer/Sterilizer/Packager/Supplier
- Expedited Review
- N
Advisory Committee Statement
ADD A SECOND IN-PROCESS CYTOTOXICITY TESTING SITE.
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 |
|---|---|---|---|
| MIP | Implanted Fecal Incontinence Device | FDA class 3 | Unknown |