Atlas FDA

+FLEX Active Electrode and Insertion Electrode (IE) FLEX

FDA premarket approval P000025/S106 · decided 2019-07-02

Approval details

PMA number
P000025
Supplement
S106
Supplement type
Normal 180 Day Track
Supplement reason
Change Design/Components/Specifications/Material
Trade name
+FLEX Active Electrode and Insertion Electrode (IE) FLEX
Generic name
Implant, cochlear
Applicant
Med-El Corp.
Date received
2018-12-17
Decision date
2019-07-02
Days to decision
197 days
Decision code
APPR
Product code
MCM
Advisory committee
Ear, Nose, Throat
Expedited review
No
Location
Innsbruck
Statement
Approval order should be issued for the +FLEX26 Active Electrode and Insertion Electrode (IE) FLEX26.

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