Atlas FDA

SynchroMed Infusion System, Ascenda® IntrathecaI Catheters

FDA premarket approval P860004/S372 · decided 2021-05-03

Approval details

PMA number
P860004
Supplement
S372
Supplement type
30-Day Notice
Supplement reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Trade name
SynchroMed Infusion System, Ascenda® IntrathecaI Catheters
Generic name
Pump, infusion, implanted, programmable
Applicant
Medtronic, Inc.
Date received
2021-04-08
Decision date
2021-05-03
Days to decision
25 days
Decision code
OK30
Product code
LKK
Advisory committee
General Hospital
Expedited review
No
Location
Minneapolis, MN
Statement
Implementation of a new Servo Press machine at Brunk Industries, Inc to manufacture the SynchroMed II Pump (SMII) Inner Shield (P/N M955170A001) for the SynchroMed Infusion System.

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510(k) clearances by this applicant

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Clearview Intracoronary Shunts (K253998)Medtronic, Inc.2026-01-20
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