Last synced on 21 February 2025 at 11:05 pm

Artificial Chordae Tendineae Surgical Replacement System

Page Type
Product Code
Definition
An artificial chordae tendineae surgical replacement system is a standalone, prescription device consisting of nonabsorbable suture-based implant and suture placement device(s) that is used to replace mitral or tricuspid chordae tendineae in patients with atrioventricular valve insufficiency. The device includes clips or fasteners to secure suture that are not embedded in the cardiac tissue. The system is used via surgical approach under direct visualization and not via transcatheter or percutaneous access.
Physical State
The implant is composed of suture and clip or fastener components that are implanted into the atrioventricular valve location using customized placement device(s).
Technical Method
The system implants suture at the atrioventricular valve target locations. The system secures the suture using clip or fastener component(s) that are not novel anchoring technologies and not embedded in the cardiac tissue. The system is used via surgical approach under direct visualization and not via transcatheter or percutaneous access.
Target Area
Mitral and Tricuspid valve apparatus
Regulation Medical Specialty
Cardiovascular
Review Panel
Cardiovascular
Submission Type
510(K)
Device Classification
Class 2
Regulation Number
870.3490
GMP Exempt?
No
Summary Malfunction Reporting
Ineligible
Implanted Device
Yes
Life-Sustain/Support Device
Yes
Third Party Review
Not Third Party Eligible

No Linked CFR Text

Product code SBK is linked to regulation 21CFR870.3490, which does not seem to exist yet. It may be pending at the moment.

Artificial Chordae Tendineae Surgical Replacement System

Page Type
Product Code
Definition
An artificial chordae tendineae surgical replacement system is a standalone, prescription device consisting of nonabsorbable suture-based implant and suture placement device(s) that is used to replace mitral or tricuspid chordae tendineae in patients with atrioventricular valve insufficiency. The device includes clips or fasteners to secure suture that are not embedded in the cardiac tissue. The system is used via surgical approach under direct visualization and not via transcatheter or percutaneous access.
Physical State
The implant is composed of suture and clip or fastener components that are implanted into the atrioventricular valve location using customized placement device(s).
Technical Method
The system implants suture at the atrioventricular valve target locations. The system secures the suture using clip or fastener component(s) that are not novel anchoring technologies and not embedded in the cardiac tissue. The system is used via surgical approach under direct visualization and not via transcatheter or percutaneous access.
Target Area
Mitral and Tricuspid valve apparatus
Regulation Medical Specialty
Cardiovascular
Review Panel
Cardiovascular
Submission Type
510(K)
Device Classification
Class 2
Regulation Number
870.3490
GMP Exempt?
No
Summary Malfunction Reporting
Ineligible
Implanted Device
Yes
Life-Sustain/Support Device
Yes
Third Party Review
Not Third Party Eligible

No Linked CFR Text

Product code SBK is linked to regulation 21CFR870.3490, which does not seem to exist yet. It may be pending at the moment.