Atlas FDA

CARELINK MONITOR SYSTEM

FDA premarket approval P890003/S178 · decided 2011-03-22

Approval details

PMA number
P890003
Supplement
S178
Supplement type
Real-Time Process
Supplement reason
Change Design/Components/Specifications/Material
Trade name
CARELINK MONITOR SYSTEM
Generic name
Pulse generator, permanent, implantable
Applicant
Medtronic, Inc.
Date received
2009-11-17
Decision date
2011-03-22
Days to decision
490 days
Decision code
APPR
Product code
NVZ
Advisory committee
Cardiovascular
Expedited review
No
Location
Mounds View, MN
Statement
APPROVAL FOR NEW APPLICATION SOFTWARE VERSION SW003 (VERSION 7.1); RELIA APPLICATION SOFTWARE VERSION SW010 (VERSION 7.1); AND CARELINK DDMA VERSION K3 DDMA1 2V4.

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