FDA-Device2023-01-18Class II
Vanta/Seqenita LT Clinician Programmer Application, Neurostimulation systems for pain therapy, Model Number CT900C
Medtronic Neuromodulation
Hazard
Software anomalies, CP App messages: "Too Many Device Found", "Unexpected Device Error Code 1502", and "System Update Needed, Service Code 303"
Sold states
Worldwide distribution.
Affected count
18 units
Manufactured in
7000 Central Ave Ne, Minneapolis, MN, United States
Products
Vanta/Seqenita LT Clinician Programmer Application, Neurostimulation systems for pain therapy, Model Number CT900C
Official notice
https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0913-2023Don't want to check this manually?
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