| Note: This medical device record is a PMA supplement. A supplement may have changed the device description/function or indication from that approved in the original PMA. Be sure to look at the original PMA record for more information. |
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| Device | CARTOID WALLSTENT MONORAIL ENDOPROSTHESIS |
| Generic Name | Stent, carotid |
| Applicant | Boston Scientific Corp Three Scimed Pl. Maple Grove, MN 55311 |
| PMA Number | P050019 |
| Supplement Number | S013 |
| Date Received | 02/04/2013 |
| Decision Date | 03/05/2013 |
| Product Code |
NIM |
| Advisory Committee |
Cardiovascular |
| Supplement Type | 30-Day Notice |
| Supplement Reason | Process Change - Manufacturer/Sterilizer/Packager/Supplier |
| Expedited Review Granted? | No |
| Combination Product | No |
| Predetermined Change Control Plan Authorized | No |
Approval Order Statement REMOVAL OF A REDUNDANT OFF-LINE INSPECTION FOR EXTRUDED COMPONENTS USED TO MANUFACTURE THE CAROTID WALLSTENT MONORAIL ENDOPROSTHESIS. |
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