Atlas FDA

Astra S DR MRI IPG, Astra S SR MRI IPG, Astra XT DR MRI IPG, Astra XT SR MRI IPG, Azure S DR MRI IPG, Azure S SR MRI IPG

FDA premarket approval P980035/S799 · decided 2024-11-20

Approval details

PMA number
P980035
Supplement
S799
Supplement type
Real-Time Process
Supplement reason
Change Design/Components/Specifications/Material
Trade name
Astra S DR MRI IPG, Astra S SR MRI IPG, Astra XT DR MRI IPG, Astra XT SR MRI IPG, Azure S DR MRI IPG, Azure S SR MRI IPG
Generic name
Pulse generator, permanent, implantable
Applicant
Medtronic, Inc.
Date received
2024-10-25
Decision date
2024-11-20
Days to decision
26 days
Decision code
APPR
Product code
NVZ
Advisory committee
Cardiovascular
Expedited review
No
Location
Mounds View, MN
Statement
Approval for changes to the manufacturing process of the electrolyte used in battery manufacturing and a temporary chloride specification excursion

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