FDA PMA FDA Class 3 Approved 🇺🇸 United States

Permanent Defibrillator Electrodes

PMA: P980023 · Supplement: S113 · Decision Jan 20, 2023
Classifications
1
FEI Numbers
36
Registration Numbers
36

Basic Information

Device Name
Permanent Defibrillator Electrodes
Trade Name
Pamira ICD Leads
PMA Number
P980023
Supplement Number
S113
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
January 20, 2023
Date Received
May 19, 2022
Supplement Type
Normal 180 Day Track
Supplement Reason
Change Design/Components/Specifications/Material
Expedited Review
N

Advisory Committee Statement

Approval for design changes to the Plexa lead family, resulting in the Pamira lead family.

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