Atlas FDA

LEGEND PLUS IPG

FDA premarket approval P930022/S017 · decided 2015-10-19

Approval details

PMA number
P930022
Supplement
S017
Supplement type
Normal 180 Day Track
Supplement reason
Change Design/Components/Specifications/Material
Trade name
LEGEND PLUS IPG
Generic name
Implantable pulse generator, pacemaker (non-CRT)
Applicant
Medtronic, Inc.
Date received
2014-12-22
Decision date
2015-10-19
Days to decision
301 days
Decision code
APPR
Product code
LWP
Advisory committee
Cardiovascular
Expedited review
No
Location
Mounds View, MN
Statement
APPROVAL FOR THE REMOTE CONTROL SOFTWARE ON THE 2090 PROGRAMMER.

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