Atlas FDA

SynchroMed Infusion System

FDA premarket approval P860004/S325 · decided 2019-09-06

Approval details

PMA number
P860004
Supplement
S325
Supplement type
Normal 180 Day Track
Supplement reason
Change Design/Components/Specifications/Material
Trade name
SynchroMed Infusion System
Generic name
Pump, infusion, implanted, programmable
Applicant
Medtronic, Inc.
Date received
2019-02-15
Decision date
2019-09-06
Days to decision
203 days
Decision code
APPR
Product code
LKK
Advisory committee
General Hospital
Expedited review
No
Location
Minneapolis, MN
Statement
Approval for spot welding additions to the motor assembly of the SynchroMed II (SMII) Implantable Drug Infusion Pump (Model 8637).

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