FDA PMA FDA Class 3 Approved 🇺🇸 United States

Permanent Defibrillator Electrodes

PMA: P920015 · Supplement: S191 · Decision May 6, 2017
Classifications
1
FEI Numbers
36
Registration Numbers
36

Basic Information

Device Name
Permanent Defibrillator Electrodes
Trade Name
MODEL 6725 IS-1 PIN PLUG
PMA Number
P920015
Supplement Number
S191
Device Class
FDA Class 3
Product Code
NVY
Generic Name
Permanent defibrillator electrodes
Medical Specialty
Unknown
Advisory Committee
Cardiovascular
Decision
Approved
Decision Code
APPR
Decision Date
May 6, 2017
Date Received
December 6, 2016
Supplement Type
Normal 180 Day Track
Supplement Reason
Change Design/Components/Specifications/Material
Expedited Review
N

Advisory Committee Statement

Approval for the Percepta/Percepta Quad, Serena/Serena Quad and Solara/Solara Quad CRT-P MRI SureScan Implantable Pulse Generators with Cardiac Resynchronization Therapy.

Classifications

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

Product Code Device Name
NVY Permanent Defibrillator Electrodes