Echo Intracranial Base Catheter
FDA 510(k) K241637 · Stryker Neurovascular
510(k) numberK241637
Submission
- Device name
- Echo Intracranial Base Catheter
- Applicant
- Stryker Neurovascular
Fremont, CA, US - Received
- June 7, 2024
- Decision date
- December 19, 2024
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
- Summary
- 510(k) summary available from FDA
Device classification
- Product code
- QJP – Catheter, Percutaneous, Neurovasculature
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 870.1250
- Specialty
- Cardiovascular
To provide vascular access to the neurovasculature for interventional or diagnostic procedures
Other 510(k)s with product code QJP
| 510(k) | Device | Applicant | Decision |
|---|---|---|---|
| K262277 | 70 NeuGlide CatheterQJP · Special | Piraeus Medical, Inc. | 09/04/2026SE |
| K261176 | Zoom 4S CatheterQJP · Traditional | Imperative Care, Inc. | 08/28/2026SE |
| K254071 | p17 XR MicrocatheterQJP · Traditional | Wallaby Medical | 08/18/2026SE |
| K260199 | SLIM MicrocatheterQJP · Traditional | Balt USA, LLC | 07/13/2026SE |
| K253901 | Millipede88 Access CatheterQJP · Traditional | Perfuze, Ltd. | 07/09/2026SE |
| K261889 | Trevo Trak 21 MicrocatheterQJP · Special | Stryker Neurovascular | 07/01/2026SE |
| K261808 | ISAAC Neurovascular Navigation CatheterQJP · Special | Microvention Inc. d/b/a Terumo Neuro | 06/30/2026SE |
| K261549 | BOBBY Balloon Guide CatheterQJP · Special | MicroVention, Inc., d/b/a Terumo Neuro | 06/09/2026SE |
| K253359 | Zenith Distal Access Long SheathQJP · Traditional | Suzhou Zenith Vascular SciTech Limited | 05/22/2026SE |
| K254178 | SAYA 86 Radial Access Guide CatheterQJP · Traditional | Asahi Intecc Co., Ltd. | 05/11/2026SE |
More from Asahi Intecc Co., Ltd.
| 510(k) | Device | Decision |
|---|---|---|
| K261889 | Trevo Trak 21 MicrocatheterQJP · Special | 07/01/2026SE |
| K253032 | AXS Lift Intracranial Base CatheterQJP · Traditional | 02/11/2026SE |
| K252694 | Target Detachable CoilHCG · Traditional | 12/11/2025SE |
| K251832 | InZone IST Detachment System; IZDS Connecting CableHCG · Special | 10/17/2025SE |
| K242289 | Excelsior XT-27 Microcatheter, Excelsior XT-27 Flex Microcatheter, Excelsior XT-27…QJP · Special | 03/21/2025SE |
| K243593 | AXS Lift Intracranial Base CatheterQJP · Traditional | 02/18/2025SE |
| K241768 | Broadway 8 CatheterQJP · Traditional | 12/19/2024SE |
| K223305 | Trevo NXT ProVue RetrieverPOL · Traditional | 03/29/2023SE |
| K222533 | Target Tetra Detachable CoilsHCG · Traditional | 12/14/2022SE |
| K211594 | Trevo Trak 21 MicrocatheterQJP · Special | 11/26/2021SE |
Questions and answers
When was Echo Intracranial Base Catheter cleared by the FDA?
Echo Intracranial Base Catheter (K241637) received a 510(k) decision of Substantially Equivalent on December 19, 2024, 195 days after the submission was received.
What is the product code of K241637?
The FDA product code is QJP – Catheter, Percutaneous, Neurovasculature, a Class II (moderate risk) device regulated under 21 CFR 870.1250.