510(k) K251668

Device
SurfRider 13 Microcatheter
Applicant
Kaneka Americas Holding, Inc.
510(k) number
K251668
Product code
QJP
Decision
Substantially Equivalent (SESE)
Decision date
2026-01-05
Date received
2025-05-30
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
Takuji Nishide
Address
7979 Gateway Blvd. Suite 220 Newark CA US 94560 94560

FDA Registration Numbers#

Source Documents#

510(k) summary PDF

Other 510(k) Records For Product Code QJP#

510(k), Device, Applicant table
510(k)DeviceApplicantDecision date
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K253032AXS Lift Intracranial Base CatheterStryker Neurovascular2026-02-11
K252297Toro 88 Superbore CatheterToro Neurovascular, Inc.2026-01-16
K251097V-DAC CatheterVesalio, Inc.2026-01-06
K252213Bendit17 MicrocatheterBend IT Technologies, Ltd.2025-12-03
K251372VersaD Delivery CatheterUnity Medical, Inc.2025-10-24
K252569Carrier XL Delivery CatheterBalt USA, LLC2025-10-22
K250960DUO MicrocatheterRev Neuro, LLC2025-09-08
K251560FUBUKI XF-R Neurovascular Long SheathAsahi Intecc Co., Ltd.2025-06-20
K251240Branchor X Balloon Guide CatheterAsahi Intecc Co., Ltd.2025-06-20