Atlas FDA

Master Intellis™ Spinal Cord Stimulation System, Vanta™ Spinal Cord Stimulation System, Inceptiv™ Spinal Cord Stimulati

FDA premarket approval P840001/S584 · decided 2024-12-05

Approval details

PMA number
P840001
Supplement
S584
Supplement type
30-Day Notice
Supplement reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Trade name
Master Intellis™ Spinal Cord Stimulation System, Vanta™ Spinal Cord Stimulation System, Inceptiv™ Spinal Cord Stimulati
Generic name
Stimulator, spinal-cord, totally implanted for pain relief
Applicant
Medtronic Neuromodulation
Date received
2024-11-19
Decision date
2024-12-05
Days to decision
16 days
Decision code
OK30
Product code
LGW
Advisory committee
Neurology
Expedited review
No
Location
Minneapolis, MN
Statement
approval for supplier, Materion, to change the manufacturing site for nickel vanadium (NiV) target products

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510(k) clearances by this applicant

RecordFirmDate
SureTune4 Software (DEN210003)Medtronic Neuromodulation2021-08-23