|
Device | PIPELINE EMBOLIZATION DEVICE, PIPELINE EMBOLIZATION DEVICE |
Generic Name | intracranial aneurysm flow diverter |
Applicant |
Micro Therapeutics, Inc. d/b/a ev3 NEUROVASCULAR |
9775 toledo way |
irvine, CA 92618 |
|
PMA Number | P100018 |
Supplement Number | S007 |
Date Received | 04/11/2013 |
Decision Date | 05/09/2013 |
Product Code |
OUT
|
Advisory Committee |
Neurology |
Supplement Type | 30-day notice |
Supplement Reason | process change - manufacturer/sterilizer/packager/supplier |
Expedited Review Granted? | No |
Combination Product |
No
|
Approval Order Statement
MANUFACTURING PROCESS CHANGE FOR THE PROTECTIVE COIL OF THE PIPELINEEMBOLIZATION DEVICE DELIVERY SYSTEM. |