PMA P100018S051

Device
Pipeline™ Flex Embolization Device (Pipeline™ Flex); Pipeline™ Flex Embolization Device with Shield Technology™ (Pipelin
Applicant
Micro Therapeutics, Inc. d/b/a ev3 Neurovascular
PMA number
P100018
Supplement
S051
Product code
OUT
Decision date
2025-06-04
Classification
Neurology
Generic name
Intracranial aneurysm flow diverter
Approval order statement
approval for sampling frequency modification for tensile testing of the pouch seal strength for the Pipeline Flex Embolization Device and Pipeline Flex Embolization Device with Shield Technology

Current openFDA PMA Record#

Device
Pipeline™ Flex Embolization Device (Pipeline™ Flex); Pipeline™ Flex Embolization Device with Shield Technology™ (Pipelin
Applicant
Micro Therapeutics, Inc. d/b/a ev3 Neurovascular
PMA number
P100018
Supplement
S051
Product code
OUT
Generic name
Intracranial aneurysm flow diverter
Decision date
2025-06-04
Decision code
OK30
Date received
2025-05-09
Supplement type
30-Day Notice
Supplement reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Approval order statement
approval for sampling frequency modification for tensile testing of the pouch seal strength for the Pipeline Flex Embolization Device and Pipeline Flex Embolization Device with Shield Technology