Atlas FDA

Neuroform Atlas® Stent System

FDA premarket approval P180031/S002 · decided 2020-01-18

Approval details

PMA number
P180031
Supplement
S002
Supplement type
Normal 180 Day Track No User Fee
Supplement reason
Postapproval Study Protocol
Trade name
Neuroform Atlas® Stent System
Generic name
Intracranial coil-assist stent
Applicant
Stryker Neurovascular
Date received
2019-08-21
Decision date
2020-01-18
Days to decision
150 days
Decision code
APPR
Product code
QCA
Advisory committee
Neurology
Expedited review
No
Location
Fremont, CA
Statement
Approval of the revised protocol for the post-approval study (PAS) protocol.

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510(k) clearances by this applicant

RecordFirmDate
Trevo Trak 21 Microcatheter (K261889)Stryker Neurovascular2026-07-01
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Excelsior XT-27 Microcatheter, Excelsior XT-27 Flex Microcatheter, Excelsior XT-27 Pre-Shaped Microcatheter, Excelsior XT-27 Flex Pre-Shaped Microcatheter (K242289)Stryker Neurovascular2025-03-21
AXS Lift Intracranial Base Catheter (K243593)Stryker Neurovascular2025-02-18
Broadway 8 Catheter (K241768)Stryker Neurovascular2024-12-19
Echo Intracranial Base Catheter (K241637)Stryker Neurovascular2024-12-19