Atlas FDA

Implantable System for Remodulin

FDA premarket approval P140032/S013 · decided 2018-08-22

Approval details

PMA number
P140032
Supplement
S013
Supplement type
Real-Time Process
Supplement reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Trade name
Implantable System for Remodulin
Generic name
Pump, infusion, implanted, programmable
Applicant
Medtronic, Inc.
Date received
2018-06-01
Decision date
2018-08-22
Days to decision
82 days
Decision code
APPR
Product code
LKK
Advisory committee
General Hospital
Expedited review
No
Location
Minneapolis, MN
Statement
Approval for a change to the XT038 TAZ series tantalum capacitor along with the required manufacturing and inspection procedure adjustments to accommodate the change.

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