Atlas FDA

Neuroform Atlas® Stent System

FDA premarket approval P180031/S005 · decided 2022-11-15

Approval details

PMA number
P180031
Supplement
S005
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
2022-09-20
Decision date
2022-11-15
Days to decision
56 days
Decision code
OK30
Product code
QCA
Advisory committee
Neurology
Expedited review
No
Location
Fremont, CA
Statement
Change to the in-process specification of the inner diameter of the nitinol stent component of the Neuroform Atlas Stent System,

Class III intelligence, same tools

PMAs share the API, exports and alerts with 510(k) data - watch an applicant and hear about every approval.

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