510(k) K241768

Device
Broadway 8 Catheter
Applicant
Stryker Neurovascular
510(k) number
K241768
Product code
QJP
Decision
Substantially Equivalent (SESE)
Decision date
2024-12-19
Date received
2024-06-20
Regulation
870.1250
Classification name
Catheter, Percutaneous, Neurovasculature
Medical specialty
Cardiovascular
Review panel
Cardiovascular
Device class
2
Clearance type
Traditional
Statement or summary
Summary
Third party reviewed
No

Applicant Contact#

Contact
Shazia Hakim
Address
47900 Bayside Pkwy. Fremont CA US 94538 94538

FDA Registration Numbers#

Source Documents#

510(k) summary PDF

Other 510(k) Records For Product Code QJP#

510(k), Device, Applicant table
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K250960DUO MicrocatheterRev Neuro, LLC2025-09-08
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