Atlas FDA

Nucleus 24 Cochlear Implant System

FDA premarket approval P970051/S218 · decided 2023-06-08

Approval details

PMA number
P970051
Supplement
S218
Supplement type
Normal 180 Day Track No User Fee
Supplement reason
Postapproval Study Protocol
Trade name
Nucleus 24 Cochlear Implant System
Generic name
Implant, cochlear
Applicant
Cochlear Americas
Date received
2023-02-16
Decision date
2023-06-08
Days to decision
112 days
Decision code
APPR
Product code
MCM
Advisory committee
Ear, Nose, Throat
Expedited review
No
Location
Lone Tree, CO
Statement
Approval of the PAS protocol for the post-approval study (PAS) protocol.

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510(k) clearances by this applicant

RecordFirmDate
Cochlear™ Osia® 3(I) Sound Processor;Cochlear™ Osia® 3 Sound Processor;Cochlear™ Osia® 3 Charger;Cochlear™ Osia® 3 Aqua+;Cochlear™ Osia® Fitting Software 3;Cochlear™ Osia® Smart App;Cochlear™ Osia® System (K260902)Cochlear Americas2026-07-10
Cochlear Osia System (K240155)Cochlear Americas2024-04-18
Instrument Case (K231604)Cochlear Americas2023-08-24
Cochlear Osia 2 System, Cochlear Osia OSI200 Implant, Cochlear Osia 2 Sound Processor, Cochlear Osia Fitting Software 2, Cochlear MRI Kit (K220922)Cochlear Americas2022-07-27
Cochlear Baha 6 System, Cochlear Baha Fitting Software 6, Cochlear Baha Baha Smart App (K212136)Cochlear Americas2021-09-29
Cochlear Baha 6 Max Sound Processor, Cochlear Baha Fitting Software 6, Cochlear Baha Smart App (K202048)Cochlear Americas2021-02-23
Cochlear Osia OSI200 Implant, Cochlear Osia 2 Sound Processor, Osia Fitting Software 2.0, Osia SmartApp, Cochlear Osia Surgical Instruments (K191921)Cochlear Americas2019-11-15
Cochlear Osia OSI100 Implant, Cochlear Osia Sound Processor, Osia Intraoperative Test Software, Osia Fitting Software, Cochlear Osia Surgical Instruments (K190589)Cochlear Americas2019-07-03