|
Device | ACTICON NEOSPHINCTER ARTIFICIAL BOWEL SPHINCTER |
Generic Name | Implanted fecal incontinence device |
Applicant | Boston Scientific Corp. 100 Boston Scientific Way Marlborough, MA 01752 |
PMA Number | P010020 |
Supplement Number | S010 |
Date Received | 07/01/2008 |
Decision Date | 08/08/2008 |
Withdrawal Date
|
12/12/2016 |
Product Code |
MIP |
Advisory Committee |
Gastroenterology/Urology |
Supplement Type | 30-Day Notice |
Supplement Reason | Process Change - Manufacturer/Sterilizer/Packager/Supplier |
Expedited Review Granted? | No |
Combination Product | No |
Recalls | CDRH Recalls |
Approval Order Statement UTILIZATION OF AN ADDITIONAL FABRICATION SYSTEM IN THE MANUFACTURING PROCESS OF THE DEVICE. |