FDA PMA FDA Class 3 Approved 🇺🇸 United States

Catheter, Percutaneous, Cardiac Ablation, For Treatment Of Atrial Flutter

PMA: P150005 · Supplement: S037 · Decision Nov 1, 2018
Classifications
1
FEI Numbers
46
Registration Numbers
46

Basic Information

Device Name
Catheter, Percutaneous, Cardiac Ablation, For Treatment Of Atrial Flutter
Trade Name
Blazer Open-Irrigated Ablation Catheter
PMA Number
P150005
Supplement Number
S037
Device Class
FDA Class 3
Product Code
OAD
Generic Name
catheter, percutaneous, cardiac ablation, for treatment of atrial flutter
Medical Specialty
Unknown
Advisory Committee
Cardiovascular
Decision
Approved
Decision Code
APPR
Decision Date
November 1, 2018
Date Received
April 27, 2018
Supplement Type
Normal 180 Day Track No User Fee
Supplement Reason
Postapproval Study Protocol
Expedited Review
N

Advisory Committee Statement

Approval for the Post-Approval Study-INTERRUPT AF Study.

Classifications

This FDA Pre-Market Approval entry is associated with 1 FDA classification via its product code.

Product Code Device Name
OAD Catheter, Percutaneous, Cardiac Ablation, For Treatment Of Atrial Flutter