FDA PMA FDA Class 3 Approved 🇺🇸 United States

Permanent Defibrillator Electrodes

PMA: P980023 · Supplement: S057 · Decision Jul 3, 2014
Classifications
1
FEI Numbers
36
Registration Numbers
36

Basic Information

Device Name
Permanent Defibrillator Electrodes
Trade Name
PROTEGO FAMILY OF ICD LEADS
PMA Number
P980023
Supplement Number
S057
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
July 3, 2014
Date Received
January 27, 2014
Supplement Type
Normal 180 Day Track
Supplement Reason
Change Design/Components/Specifications/Material
Expedited Review
N

Advisory Committee Statement

APPROVAL FOR THE DF4 VARIANTS OF THE CURRENTLY APPROVED ILESTO/IFORIAICDS/CRT-DS AND LINOXSMART ICD LEADS.

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