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Percutaneous Catheter For Cutting Or Splitting Heart Valve Leaflets Concomitant To Transcatheter Valve Procedures

Page Type
Product Code
Definition
The device is a single use percutaneous catheter system intended for mechanically splitting aortic valve leaflets that may prevent coronary artery ostia obstruction during planned transcatheter valve procedures.
Physical State
The device is a non-implantable, single-use, percutaneous catheter system with mechanical cutting element(s) at the distal end
Technical Method
The device is a single-use percutaneous catheter system that will reach the target area through the vasculature and will cut the aortic leaflet(s) using mechanical forces, such as slicing or cutting actions.
Target Area
Aortic valve leaflets, native or bioprosthetic
Regulation Medical Specialty
Cardiovascular
Review Panel
Cardiovascular
Submission Type
510(K)
Device Classification
Class 2
Regulation Number
870.1254
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 SCZ is linked to regulation 21CFR870.1254, which does not seem to exist yet. It may be pending at the moment.

Percutaneous Catheter For Cutting Or Splitting Heart Valve Leaflets Concomitant To Transcatheter Valve Procedures

Page Type
Product Code
Definition
The device is a single use percutaneous catheter system intended for mechanically splitting aortic valve leaflets that may prevent coronary artery ostia obstruction during planned transcatheter valve procedures.
Physical State
The device is a non-implantable, single-use, percutaneous catheter system with mechanical cutting element(s) at the distal end
Technical Method
The device is a single-use percutaneous catheter system that will reach the target area through the vasculature and will cut the aortic leaflet(s) using mechanical forces, such as slicing or cutting actions.
Target Area
Aortic valve leaflets, native or bioprosthetic
Regulation Medical Specialty
Cardiovascular
Review Panel
Cardiovascular
Submission Type
510(K)
Device Classification
Class 2
Regulation Number
870.1254
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 SCZ is linked to regulation 21CFR870.1254, which does not seem to exist yet. It may be pending at the moment.