Atlas FDA

Surpass Elite Flow Diverter System

FDA premarket approval P170024/S022 · decided 2025-02-12

Approval details

PMA number
P170024
Supplement
S022
Supplement type
Real-Time Process
Supplement reason
Change Design/Components/Specifications/Material
Trade name
Surpass Elite Flow Diverter System
Generic name
Intracranial aneurysm flow diverter
Applicant
Stryker Neurovascular
Date received
2024-11-26
Decision date
2025-02-12
Days to decision
78 days
Decision code
APPR
Product code
OUT
Advisory committee
Neurology
Expedited review
No
Location
Fremont, CA
Statement
Approval for a line extension for the Surpass Elite Flow Diverter System, which adds intermediate stent diameters of 3.75mm, 4.25mm, and 4.75mm.

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