Atlas FDA

Neuroform Atlas® Stent System

FDA premarket approval P180031/S008 · decided 2024-09-20

Approval details

PMA number
P180031
Supplement
S008
Supplement type
30-Day Notice
Supplement reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Trade name
Neuroform Atlas® Stent System
Generic name
Intracranial coil-assist stent
Applicant
Stryker Neurovascular
Date received
2024-09-13
Decision date
2024-09-20
Days to decision
7 days
Decision code
OK30
Product code
QCA
Advisory committee
Neurology
Expedited review
No
Location
Fremont, CA
Statement
approval for addition of a 100% in-process inspection to verify that welds of the stent delivery wire meet specifications

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510(k) clearances by this applicant

RecordFirmDate
Trevo Trak 21 Microcatheter (K261889)Stryker Neurovascular2026-07-01
AXS Lift Intracranial Base Catheter (K253032)Stryker Neurovascular2026-02-11
Target Detachable Coil (K252694)Stryker Neurovascular2025-12-11
InZone IST Detachment System; IZDS Connecting Cable (K251832)Stryker Neurovascular2025-10-17
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