FDA PMA FDA Class 3 Approved 🇺🇸 United States

Implantable Pulse Generator, Pacemaker (Non-Crt)

PMA: P140033 · Supplement: S067 · Decision Jun 28, 2021
Classifications
1
FEI Numbers
35
Registration Numbers
35

Basic Information

Device Name
Implantable Pulse Generator, Pacemaker (Non-Crt)
Trade Name
Assurity MRI, Endurity MRI family of Pacemakers
PMA Number
P140033
Supplement Number
S067
Device Class
FDA Class 3
Product Code
LWP
Generic Name
Implantable pulse generator, pacemaker (non-CRT)
Medical Specialty
Unknown
Advisory Committee
Cardiovascular
Decision
Approved
Decision Code
APPR
Decision Date
June 28, 2021
Date Received
April 2, 2021
Supplement Type
Real-Time Process
Supplement Reason
Change Design/Components/Specifications/Material
Expedited Review
N

Advisory Committee Statement

Approval for changes to the Merlin PCS 3650 Programmer Model 3330 Software to create v25.1.1.

Classifications

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

Product Code Device Name
LWP Implantable Pulse Generator, Pacemaker (Non-Crt)