Stryker Neurovascular - FDA 510(k) Cleared Devices
32
Total
32
Cleared
0
Denied
Stryker Neurovascular has 32 FDA 510(k) cleared neurology devices. Based in Freemont, US.
Latest FDA clearance: Feb 2026. Active since 2011.
Browse the complete list of FDA 510(k) cleared neurology devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Stryker Neurovascular
32 devices
Cleared
Feb 11, 2026
AXS Lift Intracranial Base Catheter
Neurology
142d
Cleared
Dec 11, 2025
Target Detachable Coil
Neurology
107d
Cleared
Oct 17, 2025
InZone IST Detachment System
Neurology
123d
Cleared
Mar 21, 2025
Excelsior XT-27 Microcatheter, Excelsior XT-27 Flex Microcatheter, Excelsior...
Neurology
231d
Cleared
Feb 18, 2025
AXS Lift Intracranial Base Catheter
Neurology
90d
Cleared
Dec 19, 2024
Echo Intracranial Base Catheter
Neurology
195d
Cleared
Dec 19, 2024
Broadway 8 Catheter
Neurology
182d
Cleared
Mar 29, 2023
Trevo NXT ProVue Retriever
Neurology
153d
Cleared
Dec 14, 2022
Target Tetra Detachable Coils
Neurology
114d
Cleared
Nov 26, 2021
Trevo Trak 21 Microcatheter
Neurology
186d
Cleared
Nov 16, 2021
InZone Detachment System
Neurology
103d
Cleared
Aug 27, 2021
AXS Vecta 46 Intermediate Catheter
Neurology
340d