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FDA 510(k)

AXS Lift Intracranial Base Catheter

K-Number: K243593 · 2025-02-18

ApplicantStryker Neurovascular
Decision Date2025-02-18
Product CodeQJP
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

AXS Lift Intracranial Base Catheter is a medical device manufactured by Stryker Neurovascular. It received FDA 510(k) clearance on 2025-02-18 under approval number K243593. The device is classified under product code QJP. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AXS Lift Intracranial Base Catheter?

AXS Lift Intracranial Base Catheter is a medical device that received FDA 510(k) clearance on 2025-02-18. It is manufactured by Stryker Neurovascular. The 510(k) number is K243593.

When was AXS Lift Intracranial Base Catheter approved by the FDA?

AXS Lift Intracranial Base Catheter received FDA 510(k) clearance on 2025-02-18, under approval number K243593.

What company makes AXS Lift Intracranial Base Catheter?

AXS Lift Intracranial Base Catheter is manufactured by Stryker Neurovascular.

What is the FDA product code for AXS Lift Intracranial Base Catheter?

The FDA product code for AXS Lift Intracranial Base Catheter is QJP.

Related Clinical Trials

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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