Atlas FDA

IsoMed Infusion System

FDA premarket approval P990034/S039 · decided 2020-03-23

Approval details

PMA number
P990034
Supplement
S039
Supplement type
Normal 180 Day Track
Supplement reason
Labeling Change - Indications/instructions/shelf life/tradename
Trade name
IsoMed Infusion System
Generic name
Pump, infusion, implanted, programmable
Applicant
Medtronic, Inc.
Date received
2019-07-12
Decision date
2020-03-23
Days to decision
255 days
Decision code
APPR
Product code
LKK
Advisory committee
General Hospital
Expedited review
No
Location
Minneapolis, MN
Statement
Approval for labeling changes for the Synchromed II and Isomed infusion systems including clarifications of the Ascenda catheter implant technique, the development of a standalone MRI guideline manual and updates to adverse event labeling/minor administrative changes.

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