510(k) K242392

Device
PATH BGC
Applicant
Crossroads Neurovascular, Inc.
510(k) number
K242392
Product code
QJP
Decision
Substantially Equivalent (SESE)
Decision date
2025-05-09
Date received
2024-08-12
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
N

Related Records

Applicant Contact

Contact
Ryan Breckenridge
Address
105 N. Pt.e Dr., Suite D Lake Forest CA US 92630 92630

FDA Registration Numbers

Source Documents

510(k) summary PDF

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