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

Permanent Defibrillator Electrodes

PMA: P920015 · Supplement: S208 · Decision Mar 20, 2018
Classifications
1
FEI Numbers
36
Registration Numbers
36

Basic Information

Device Name
Permanent Defibrillator Electrodes
Trade Name
6996T Tunneling Tool Sterile Barrier System
PMA Number
P920015
Supplement Number
S208
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
March 20, 2018
Date Received
February 22, 2018
Supplement Type
30-Day Notice
Supplement Reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Expedited Review
N

Advisory Committee Statement

Addition of packaging and sterilization processes at the Rice Creek facility as well as minor process and sterilization changes for the Model 6996T tunneling tool.

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