Last synced on 21 February 2025 at 11:05 pm

Temporary Embolization Assist Device, Peripheral

Page Type
Product Code
Definition
A temporary coil embolization assist device is a prescription device intended for temporary use in the vasculature to mechanically assist in the embolization of aneurysms with embolic coils. The device is delivered into the vasculature with an endovascular approach. This device is not intended to be permanently implanted and is removed from the body when the procedure is completed.
Physical State
The device is composed of a wire mesh stent permanently affixed to end the end of a pusher wire. Once in place the internal core wire with drawn distally which expands the mesh and blocks the neck of the aneurysm.
Technical Method
The device acts as a temporary bridge used to aid in the coiling processes while minimizing the risk of coil protrusion or prolapse. Once the coiling procedure is completed the device is removed from the parent artery.
Target Area
This device is used to treat aneurysms.
Regulation Medical Specialty
Cardiovascular
Review Panel
Cardiovascular
Submission Type
510(K)
Device Classification
Class 2
Regulation Number
870.3325
GMP Exempt?
No
Summary Malfunction Reporting
Ineligible
Implanted Device
No
Life-Sustain/Support Device
No
Third Party Review
Not Third Party Eligible

No Linked CFR Text

Product code QZU is linked to regulation 21CFR870.3325, which does not seem to exist yet. It may be pending at the moment.

Temporary Embolization Assist Device, Peripheral

Page Type
Product Code
Definition
A temporary coil embolization assist device is a prescription device intended for temporary use in the vasculature to mechanically assist in the embolization of aneurysms with embolic coils. The device is delivered into the vasculature with an endovascular approach. This device is not intended to be permanently implanted and is removed from the body when the procedure is completed.
Physical State
The device is composed of a wire mesh stent permanently affixed to end the end of a pusher wire. Once in place the internal core wire with drawn distally which expands the mesh and blocks the neck of the aneurysm.
Technical Method
The device acts as a temporary bridge used to aid in the coiling processes while minimizing the risk of coil protrusion or prolapse. Once the coiling procedure is completed the device is removed from the parent artery.
Target Area
This device is used to treat aneurysms.
Regulation Medical Specialty
Cardiovascular
Review Panel
Cardiovascular
Submission Type
510(K)
Device Classification
Class 2
Regulation Number
870.3325
GMP Exempt?
No
Summary Malfunction Reporting
Ineligible
Implanted Device
No
Life-Sustain/Support Device
No
Third Party Review
Not Third Party Eligible

No Linked CFR Text

Product code QZU is linked to regulation 21CFR870.3325, which does not seem to exist yet. It may be pending at the moment.