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AXS Lift Intracranial Base Catheter

by Stryker Neurovascular 2 variants

510(k) K253032

Active United States

510(k)

Valid until

No expiry

510(k) clearance is not time-limited

FDA recalls

None found

in data synced 22 Oct 2026

Documents

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source FDA 510(k), synced 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesFDA 510(k)SESE Substantially Equivalent · Traditional NumberK253032 Date11 Feb 2026ClearedStatusActive

Recalls

0 recalls · FDA

No FDA recalls found in the data synced 22 Oct 2026.

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — FDA 510(k) Active

Specification

510(k)

510(k) Number
FDA Product Code
QJP
Device Class
Class II
Regulation
21 CFR Part 870.1250
Advisory Committee
Cardiovascular
FDA Decision
SESE Substantially Equivalent

Overview

AI-generated summary, 24 Sep 2026

Written by a language model from registry data. Not verified by deviCERTS or the manufacturer. The registry data above is the record.

The AXS Lift Intracranial Base Catheter is a percutaneous neurovascular catheter designed to provide access and stable support from groin puncture to the cavernous segment of the internal carotid artery (ICA). It combines the simplicity of a biaxial setup with the support of a triaxial system for neurovascular access and delivery of interventional therapies.

This device is supplied as a single-use catheter and is intended for use in cardiovascular procedures. It has received FDA 510(k) clearance with the product code QJP and is classified as a Class II device. The catheter is manufactured by Stryker Neurovascular and is designed to be used in a clinical setting under appropriate regulatory authorizations.

From the manufacturer

AXS Lift is the first of its kind intracranial base catheter designed to give you the simplicity of a biaxial setup with the support of a triaxial system.

Source: stryker.com

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Questions

AI-generated answers, 24 Sep 2026

Written by a language model from registry data. Not verified by deviCERTS or the manufacturer. The registry data above is the record.

  • What is the AXS Lift Intracranial Base Catheter used for?

    The AXS Lift Intracranial Base Catheter is a percutaneous neurovascular catheter designed to provide access and stable support from groin puncture to the cavernous segment of the internal carotid artery (ICA) for neurovascular procedures.

  • Is the AXS Lift Intracranial Base Catheter single-use or reusable?

    The AXS Lift Intracranial Base Catheter is supplied as a single-use device and should not be reused to ensure patient safety and device performance.

  • What regulatory approvals does the AXS Lift Intracranial Base Catheter have?

    The AXS Lift Intracranial Base Catheter has received FDA 510(k) clearance with product code QJP and is classified as a Class II device for cardiovascular procedures.

  • How is the AXS Lift Intracranial Base Catheter different from other neurovascular catheters?

    The AXS Lift Intracranial Base Catheter combines the simplicity of a biaxial setup with the support of a triaxial system, providing stable access from the groin to the cavernous segment of the internal carotid artery.