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CARELINK PROGRAMMER CRM PROGRAMMER

FDA premarket approval P890003/S242 · decided 2011-12-21

Approval details

PMA number
P890003
Supplement
S242
Supplement type
Real-Time Process
Supplement reason
Change Design/Components/Specifications/Material
Trade name
CARELINK PROGRAMMER CRM PROGRAMMER
Generic name
Pulse generator, permanent, implantable
Applicant
Medtronic, Inc.
Date received
2011-11-25
Decision date
2011-12-21
Days to decision
26 days
Decision code
APPR
Product code
NVZ
Advisory committee
Cardiovascular
Expedited review
No
Location
Mounds View, MN
Statement
APPROVAL FOR COMPONENTS CHANGING FROM LEAD-CONTAINING TO LEAD-FREE USED IN THE MEDTRONIC 2090 PROGRAMMER, 5388 DUAL CHAMBER EPG, AND 5348 SINGLE CHAMBER EPG.

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