Atlas FDA

Neuroform Atlas Stent System

FDA premarket approval P180031/S011 · decided 2025-05-09

Approval details

PMA number
P180031
Supplement
S011
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
2025-04-10
Decision date
2025-05-09
Days to decision
29 days
Decision code
OK30
Product code
QCA
Advisory committee
Neurology
Expedited review
No
Location
Fremont, CA
Statement
to introduce a new degreaser solvent to use in the manufacture of the Radiopaque Marker Band

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