Atlas FDA

Evoke® SCS System

FDA premarket approval P190002/S024 · decided 2024-02-29

Approval details

PMA number
P190002
Supplement
S024
Supplement type
30-Day Notice
Supplement reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Trade name
Evoke® SCS System
Generic name
Stimulator, spinal-cord, totally implanted for pain relief
Applicant
Saluda Medical Pty, Ltd.
Date received
2024-01-31
Decision date
2024-02-29
Days to decision
29 days
Decision code
OK30
Product code
LGW
Advisory committee
Neurology
Expedited review
No
Location
Atarmon
Statement
the expansion of an existing clean room to support increased manufacturing capacity of the contract manufacturer for lead and lead accessories for the Evoke SCS System

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