Atlas FDA

Optune

FDA premarket approval P100034/S030 · decided 2024-01-16

Approval details

PMA number
P100034
Supplement
S030
Supplement type
Normal 180 Day Track
Supplement reason
Change Design/Components/Specifications/Material
Trade name
Optune
Generic name
Stimulator, low electric field, tumor treatment
Applicant
Novocure, GmbH
Date received
2023-01-25
Decision date
2024-01-16
Days to decision
356 days
Decision code
APPR
Product code
NZK
Advisory committee
Neurology
Expedited review
No
Location
Baar
Statement
approval for the MAXPOINT BR-I (“MAXPOINT”) Optune transducer array layout software

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