FDA PMA FDA Class 3 Approved 🇺🇸 United States

Permanent Defibrillator Electrodes

PMA: P920015 · Supplement: S204 · Decision Mar 1, 2018
Classifications
1
FEI Numbers
36
Registration Numbers
36

Basic Information

Device Name
Permanent Defibrillator Electrodes
Trade Name
Sprint Quattro Secure S MRI SureScan Lead & Sprint Quattro Secure MRI SureScan Lead
PMA Number
P920015
Supplement Number
S204
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
March 1, 2018
Date Received
December 4, 2017
Supplement Type
Real-Time Process
Supplement Reason
Change Design/Components/Specifications/Material
Expedited Review
N

Advisory Committee Statement

Approval for the addition of the Primo MRI SureScan and Mirro MRI SureScan ICDs to the Evera MRI Conditional family of devices.

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