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KAPPA 400 DR & SR IPG PACEMAKERS

FDA premarket approval P970012/S038 · decided 2008-11-21

Approval details

PMA number
P970012
Supplement
S038
Supplement type
Normal 180 Day Track
Supplement reason
Change Design/Components/Specifications/Material
Trade name
KAPPA 400 DR & SR IPG PACEMAKERS
Generic name
Pulse generator, permanent, implantable
Applicant
Medtronic, Inc.
Date received
2008-07-28
Decision date
2008-11-21
Days to decision
116 days
Decision code
APPR
Product code
NVZ
Advisory committee
Cardiovascular
Expedited review
No
Location
Mounds View, MN
Statement
APPROVAL FOR COMPONENT, DESIGN, MANUFACTURING PROCESS, AND LABELING UPDATES TO THE MEDTRONIC 2090 CARELINK PROGRAMMER, WHICH ARE DRIVEN BY COMPONENT OBSOLESCENCE. UPDATES INCLUDE A NEW TOUCH SCREEN, A NEW LIQUID CRYSTAL DISPLAY (LCD), A LOCAL AREA NETWORK (LAN) ON THE MICRO-PROCESSING UNIT (MPU), NEW HARD DRIVES, UPDATES TO THE LINK ELECTRONICS MODULE (LEM), AND OTHER MINOR CHANGES TO ADDRESS OBSOLETE COMPONENTS.

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