Last synced on 25 January 2026 at 3:41 am

Echo Intracranial Base Catheter

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K241637
510(k) Type
Traditional
Applicant
Stryker Neurovascular
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/19/2024
Days to Decision
195 days
Submission Type
Summary

Echo Intracranial Base Catheter

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K241637
510(k) Type
Traditional
Applicant
Stryker Neurovascular
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/19/2024
Days to Decision
195 days
Submission Type
Summary