FDA PMA FDA Class 3 30-Day Notice Accepted 🇺🇸 United States

Permanent Defibrillator Electrodes

PMA: P920015 · Supplement: S259 · Decision Aug 17, 2021
Classifications
1
FEI Numbers
36
Registration Numbers
36

Basic Information

Device Name
Permanent Defibrillator Electrodes
Trade Name
Y Adaptor/Extender Kit, DF-1 Connector Port Pin Plug, HV Splitter/Adaptor Kit, IS-1 Connector Port Pin Plug Kit, Lead Ad
PMA Number
P920015
Supplement Number
S259
Device Class
FDA Class 3
Product Code
NVY
Generic Name
Permanent defibrillator electrodes
Medical Specialty
Unknown
Advisory Committee
Cardiovascular
Decision
30-Day Notice Accepted
Decision Code
OK30
Decision Date
August 17, 2021
Date Received
August 9, 2021
Supplement Type
30-Day Notice
Supplement Reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Expedited Review
N

Advisory Committee Statement

Minor modifications, including new ovens and a new toolmaker's scope at Medtronic Rice Creek.

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