Atlas FDA

CapSureFix MRI SureScan Lead

FDA premarket approval P090013/S293 · decided 2019-04-10

Approval details

PMA number
P090013
Supplement
S293
Supplement type
Normal 180 Day Track
Supplement reason
Change Design/Components/Specifications/Material
Trade name
CapSureFix MRI SureScan Lead
Generic name
Implantable pulse generator, pacemaker (non-CRT)
Applicant
Medtronic, Inc.
Date received
2018-10-26
Decision date
2019-04-10
Days to decision
166 days
Decision code
APPR
Product code
LWP
Advisory committee
Cardiovascular
Expedited review
No
Location
Mounds View, MN
Statement
Approval for the Attain Stability™ Quad MRI SureScan™ Model 4798 left ventricular (LV) lead.

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