PMA P010020S014
- Device
- ACTICON NEOSPHINCTER ARTIFICAL BOWEL SPHINCTER
- Applicant
- Boston Scientific Corp
- PMA number
- P010020
- Supplement
- S014
- Product code
- MIP
- Decision date
- 2009-08-13
- Classification
- Gastroenterology, Urology
- Generic name
- Implanted fecal incontinence device
- Approval order statement
- REPLACEMENT OF DIPPING EQUIPMENT USED IN THE MANUFACTURE OF THE DEVICES.
Current openFDA PMA Record#
- Device
- ACTICON NEOSPHINCTER ARTIFICAL BOWEL SPHINCTER
- Applicant
- Boston Scientific Corp
- PMA number
- P010020
- Supplement
- S014
- Product code
- MIP
- Generic name
- Implanted fecal incontinence device
- Decision date
- 2009-08-13
- Decision code
- OK30
- Date received
- 2009-07-14
- Supplement type
- 30-Day Notice
- Supplement reason
- Process Change - Manufacturer/Sterilizer/Packager/Supplier
- Approval order statement
- REPLACEMENT OF DIPPING EQUIPMENT USED IN THE MANUFACTURE OF THE DEVICES.