Last synced on 10 January 2025 at 11:05 pm

Brain Intraparenchymal Infusion Cannula

Page Type
Product Code
Definition
A brain intraparenchymal infusion cannula is a non-powered, hollow tube-like device with a rigid component for stereotaxic-aided temporary placement in brain parenchyma tissue to deliver a therapy.
Physical State
A brain intraparenchymal infusion cannula is a non-powered, hollow tube-like device made of various materials (e.g., ceramics, polymers, or metals).
Technical Method
A brain intraparenchymal infusion cannula is guided to a target in the brain by stereotaxic navigation and used to deliver a therapy (e.g., biologic or drug product) by connection of the cannula to an infusion pump system.
Target Area
Brain parenchyma tissue.
Regulation Medical Specialty
Neurology
Review Panel
Neurology
Submission Type
510(K)
Device Classification
Class 2
Regulation Number
882.4110
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 SDG is linked to regulation 21CFR882.4110, which does not seem to exist yet. It may be pending at the moment.

Brain Intraparenchymal Infusion Cannula

Page Type
Product Code
Definition
A brain intraparenchymal infusion cannula is a non-powered, hollow tube-like device with a rigid component for stereotaxic-aided temporary placement in brain parenchyma tissue to deliver a therapy.
Physical State
A brain intraparenchymal infusion cannula is a non-powered, hollow tube-like device made of various materials (e.g., ceramics, polymers, or metals).
Technical Method
A brain intraparenchymal infusion cannula is guided to a target in the brain by stereotaxic navigation and used to deliver a therapy (e.g., biologic or drug product) by connection of the cannula to an infusion pump system.
Target Area
Brain parenchyma tissue.
Regulation Medical Specialty
Neurology
Review Panel
Neurology
Submission Type
510(K)
Device Classification
Class 2
Regulation Number
882.4110
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 SDG is linked to regulation 21CFR882.4110, which does not seem to exist yet. It may be pending at the moment.