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. |
|
Device | FLEXTOME CUTTING BALLOON DILATATION DEVICE |
Generic Name | STENT, CORONARY |
Applicant | Boston Scientific Corp. ONE SCIMED PLACE MAPLE GROVE, MN 55311-1566 |
PMA Number | P950020 |
Supplement Number | S067 |
Date Received | 01/17/2014 |
Decision Date | 02/13/2014 |
Product Code |
MAF |
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 ADD A FIXTURE TO THE LASER USED IN THE HYPOTUBE-COREWIRE LASER BONDING STEP OF THE BALLOON CATHETER MANUFACTURING PROCESS. |
|
|