FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

AXS Lift Intracranial Base Catheter

K Number: K253032 · Decision Feb 11, 2026
Classifications
1
FEI Numbers
72
Registration Numbers
72
Same Product Code
91
Applicant Total
32
Review Days
142

Basic Information

Device Name
AXS Lift Intracranial Base Catheter
K Number
K253032
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.1250
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Stryker Neurovascular
Date Received
September 22, 2025
Decision Date
February 11, 2026
Product Code
QJP
Advisory Committee
Cardiovascular
Review Advisory Committee
NE
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
QJP Catheter, Percutaneous, Neurovasculature

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