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CRT-D RESYNCHRONIZATION DEVICES, COGNIS, ENERGEN, PUNCTUA, INCEPTA, ORIGEN, INOGEN, DYNAGEN, AUTOGEN

FDA premarket approval P010012/S417 · decided 2016-07-08

Approval details

PMA number
P010012
Supplement
S417
Supplement type
Real-Time Process
Supplement reason
Change Design/Components/Specifications/Material
Trade name
CRT-D RESYNCHRONIZATION DEVICES, COGNIS, ENERGEN, PUNCTUA, INCEPTA, ORIGEN, INOGEN, DYNAGEN, AUTOGEN
Generic name
Defibrillator, automatic implantable cardioverter, with cardiac resynchronization (CRT-D)
Applicant
Boston Scientific Corp
Date received
2016-04-21
Decision date
2016-07-08
Days to decision
78 days
Decision code
APPR
Product code
NIK
Advisory committee
Cardiovascular
Expedited review
No
Location
St Paul, MN
Statement
Approval for LATITUDE NXT Patient Management System, Release 4.1.1.

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