FDA PMA FDA Class 3 Approved 🇺🇸 United States

Implantable Pacemaker Pulse-Generator

PMA: P880086 · Supplement: S272 · Decision Jun 28, 2016
Classifications
1
FEI Numbers
28
Registration Numbers
28

Basic Information

Device Name
Implantable Pacemaker Pulse-Generator
Trade Name
ACCENT, IDENTITY, VERITY, VICTORY AND ZEPHYR PACEMAKERS
PMA Number
P880086
Supplement Number
S272
Device Class
FDA Class 3
Product Code
DXY
Generic Name
implantable pacemaker Pulse-generator
Regulation Number
870.3610
Medical Specialty
Cardiovascular
Advisory Committee
Cardiovascular
Decision
Approved
Decision Code
APPR
Decision Date
June 28, 2016
Date Received
April 4, 2016
Supplement Type
Real-Time Process
Supplement Reason
Change Design/Components/Specifications/Material
Expedited Review
N

Advisory Committee Statement

Approval for Merlin PCS Model 3330 v22.0.1 Software.

Classifications

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

Product Code Device Name
DXY Implantable Pacemaker Pulse-Generator