FDA PMA FDA Class 3 Approved 🇺🇸 United States

Implantable Pacemaker Pulse-Generator

PMA: P880086 · Supplement: S325 · Decision Sep 30, 2022
Classifications
1
FEI Numbers
28
Registration Numbers
28

Basic Information

Device Name
Implantable Pacemaker Pulse-Generator
Trade Name
Assurity, Assurity+, Endurity, Accent family of Pacemakers
PMA Number
P880086
Supplement Number
S325
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
September 30, 2022
Date Received
July 27, 2022
Supplement Type
Real-Time Process
Supplement Reason
Change Design/Components/Specifications/Material
Expedited Review
N

Advisory Committee Statement

Approval for the Merlin@home transmitter software model EX2000 v9.0 and cybersecurity enhancements.

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