PMA P100018S036

Device
Pipeline™ Flex Embolization Device, Pipeline™ Flex Embolization Device with Shield Technology™
Applicant
Micro Therapeutics, Inc. d/b/a ev3 Neurovascular
PMA number
P100018
Supplement
S036
Product code
OUT
Decision date
2021-12-27
Generic name
Intracranial aneurysm flow diverter
Approval order statement
Relocation of the distal bump wire supplier, Creganna Medical, from the manufacturing location in Tualatin, Oregon, to Wilsonville, Oregon.

Current openFDA PMA Record#

Device
Pipeline™ Flex Embolization Device, Pipeline™ Flex Embolization Device with Shield Technology™
Applicant
Micro Therapeutics, Inc. d/b/a ev3 Neurovascular
PMA number
P100018
Supplement
S036
Product code
OUT
Generic name
Intracranial aneurysm flow diverter
Decision date
2021-12-27
Decision code
OK30
Date received
2021-12-08
Supplement type
30-Day Notice
Supplement reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Approval order statement
Relocation of the distal bump wire supplier, Creganna Medical, from the manufacturing location in Tualatin, Oregon, to Wilsonville, Oregon.