FDA PMA FDA Class 3 Approved 🇺🇸 United States

Mitral Valve Repair Devices

PMA: P100009 · Supplement: S017 · Decision Mar 30, 2016
Classifications
1
FEI Numbers
18
Registration Numbers
18

Basic Information

Device Name
Mitral Valve Repair Devices
Trade Name
MITRACLIP DELIVERY SYSTEM
PMA Number
P100009
Supplement Number
S017
Device Class
FDA Class 3
Product Code
NKM
Generic Name
Mitral valve repair devices
Medical Specialty
Unknown
Advisory Committee
Cardiovascular
Decision
Approved
Decision Code
APPR
Decision Date
March 30, 2016
Date Received
March 1, 2016
Supplement Type
Special (Immediate Track)
Supplement Reason
Labeling Change - Indications/instructions/shelf life/tradename
Expedited Review
N

Advisory Committee Statement

Approval to modify the deployment sequence instructions in the Instructions for Use.

Classifications

This FDA Pre-Market Approval entry is associated with 1 FDA classification via its product code.

Product Code Device Name
NKM Mitral Valve Repair Devices