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Consulta CRT-P C4TR01; Syncra CRT-P C2TR01; Viva CRT-P C6TR01

FDA premarket approval P010015/S298 · decided 2016-04-22

Approval details

PMA number
P010015
Supplement
S298
Supplement type
30-Day Notice
Supplement reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Trade name
Consulta CRT-P C4TR01; Syncra CRT-P C2TR01; Viva CRT-P C6TR01
Generic name
Implantable pulse generator, pacemaker (non-CRT)
Applicant
Medtronic, Inc.
Date received
2016-03-31
Decision date
2016-04-22
Days to decision
22 days
Decision code
OK30
Product code
LWP
Advisory committee
Cardiovascular
Expedited review
No
Location
Mounds View, MN
Statement
Add an alternate material for a manufacturing gauge tool.

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