Atlas FDA

Surpass Streamline Flow Diverter

FDA premarket approval P170024/S001 · decided 2018-10-05

Approval details

PMA number
P170024
Supplement
S001
Supplement type
30-Day Notice
Supplement reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Trade name
Surpass Streamline Flow Diverter
Generic name
Intracranial aneurysm flow diverter
Applicant
Stryker Neurovascular
Date received
2018-09-20
Decision date
2018-10-05
Days to decision
15 days
Decision code
OK30
Product code
OUT
Advisory committee
Neurology
Expedited review
No
Location
Fremont, CA
Statement
Reduction of the frequency of in-process inspection for the pouch sealing process to once daily.

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