Atlas FDA

CapSure VDD-2 Lead, CareLink SmartSync Device Manager Programmer, Service Kit-Pacemaker Repair Kit, Vitatron Brilliant S

FDA premarket approval P890003/S450 · decided 2021-12-07

Approval details

PMA number
P890003
Supplement
S450
Supplement type
30-Day Notice
Supplement reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Trade name
CapSure VDD-2 Lead, CareLink SmartSync Device Manager Programmer, Service Kit-Pacemaker Repair Kit, Vitatron Brilliant S
Generic name
Pulse generator, permanent, implantable
Applicant
Medtronic, Inc.
Date received
2021-11-18
Decision date
2021-12-07
Days to decision
19 days
Decision code
OK30
Product code
NVZ
Advisory committee
Cardiovascular
Expedited review
No
Location
Mounds View, MN
Statement
Update the manufacturing execution system (MES) to FACTORYworks (FW) Release 9.9.

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