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Drug Delivery Infusion Pumps SynchroMed

FDA premarket approval P860004/S349 · decided 2020-01-09

Approval details

PMA number
P860004
Supplement
S349
Supplement type
30-Day Notice
Supplement reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Trade name
Drug Delivery Infusion Pumps SynchroMed
Generic name
Pump, infusion, implanted, programmable
Applicant
Medtronic, Inc.
Date received
2019-12-10
Decision date
2020-01-09
Days to decision
30 days
Decision code
OK30
Product code
LKK
Advisory committee
General Hospital
Expedited review
No
Location
Minneapolis, MN
Statement
Changes to the manufacturing process (i.e., copper plating, additional solder mask developing line) for the printed wiring board (PWB) provided from an external supplier.

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510(k) clearances by this applicant

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