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 | INCEPTA,ENERGEN,PUNCTUA,COGNIS CRT-DS |
Generic Name | Implantable pulse generator, pacemaker (non-CRT) |
Applicant | Boston Scientific Corp. 4100 HAMLINE AVE NORTH ST. PAUL, MN 55112 |
PMA Number | P010012 |
Supplement Number | S327 |
Date Received | 04/01/2013 |
Decision Date | 04/26/2013 |
Product Code |
LWP |
Advisory Committee |
Cardiovascular |
Supplement Type | 30-Day Notice |
Expedited Review Granted? | No |
Combination Product | No |
Approval Order Statement OPTIMIZATION OF WELD PROCESS PARAMETERS AND REMOVAL OF A WELD INSPECTION CRITERION FOR THE DEVICES. |
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