510(k) K232955

Device
Numen Coil Embolization System; NumenFR Detachment System
Applicant
MicroPort NeuroTech (Shanghai) Co., Ltd.
510(k) number
K232955
Product code
HCG
Decision
Substantially Equivalent (SESE)
Decision date
2024-01-10
Date received
2023-09-21
Regulation
882.5950
Classification name
Device, Neurovascular Embolization
Medical specialty
Neurology
Review panel
Neurology
Device class
2
Clearance type
Special
Statement or summary
Summary
Third party reviewed
No

Related Records

Applicant Contact

Contact
Jiayin Sun
Address
16th Bldg. , 222 Guangdan Rd., Pudong New District Shanghai CN 201318 201318

FDA Registration Numbers

Source Documents

510(k) summary PDF

Other 510(k) Records For Product Code HCG

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K212455InZone Detachment SystemStryker Neurovascular2021-11-16
K203625Numen Coil Embolization System; NumenFR Detachment SystemMicroPort NeuroTech (Shanghai) Co., Ltd.2021-09-01