Atlas FDA

Pulse Generator, Permanent Implantable (Device Reader/Interrogator)

FDA premarket approval P890003/S395 · decided 2018-10-18

Approval details

PMA number
P890003
Supplement
S395
Supplement type
Real-Time Process
Supplement reason
Change Design/Components/Specifications/Material
Trade name
Pulse Generator, Permanent Implantable (Device Reader/Interrogator)
Generic name
Pulse generator, permanent, implantable
Applicant
Medtronic, Inc.
Date received
2018-08-22
Decision date
2018-10-18
Days to decision
57 days
Decision code
APPR
Product code
NVZ
Advisory committee
Cardiovascular
Expedited review
No
Location
Mounds View, MN
Statement
Approval for updates to the remote monitoring systems for Attesta and Sphera MRI SureScan IPG devices.

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