Atlas FDA

CareLink SmartSync Device Manager

FDA premarket approval P980035/S583 · decided 2019-06-04

Approval details

PMA number
P980035
Supplement
S583
Supplement type
Real-Time Process
Supplement reason
Change Design/Components/Specifications/Material
Trade name
CareLink SmartSync Device Manager
Generic name
Pulse generator, permanent, implantable
Applicant
Medtronic, Inc.
Date received
2019-03-18
Decision date
2019-06-04
Days to decision
78 days
Decision code
APPR
Product code
NVZ
Advisory committee
Cardiovascular
Expedited review
No
Location
Mounds View, MN
Statement
Approval for updates to the Medtronic CareLink SmartSync Azure Astra Application and updates to the CareLink SmartSync Device Manager.

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