FDA PMA FDA Class 3 Approved 🇺🇸 United States

Implantable Pacemaker Pulse-Generator

PMA: P880086 · Supplement: S280 · Decision Oct 20, 2017
Classifications
1
FEI Numbers
28
Registration Numbers
28

Basic Information

Device Name
Implantable Pacemaker Pulse-Generator
Trade Name
Assurity, Endurity, Accent, AddVent, Identity, Entity, Paragon III Sustain
PMA Number
P880086
Supplement Number
S280
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
October 20, 2017
Date Received
February 7, 2017
Supplement Type
Real-Time Process
Supplement Reason
Change Design/Components/Specifications/Material
Expedited Review
N

Advisory Committee Statement

Approval for the Merlin Patient Care System (PCS) Model 3330 version 23.0.1 Software for the Merlin PCS Model 3650 Programmer.

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