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 Place Maple Grove, MN 55311-1566 |
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 |
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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