Atlas FDA

NUCLEUS 22 CHANNEL COCHLEAR IMPLANT SYSTEM

FDA premarket approval P890027/S041 · decided 1998-06-26

Approval details

PMA number
P890027
Supplement
S041
Supplement type
Normal 180 Day Track
Supplement reason
Change Design/Components/Specifications/Material
Trade name
NUCLEUS 22 CHANNEL COCHLEAR IMPLANT SYSTEM
Generic name
Implant, cochlear
Applicant
Cochlear Americas
Date received
1997-10-02
Decision date
1998-06-26
Days to decision
267 days
Decision code
APPR
Product code
MCM
Advisory committee
Ear, Nose, Throat
Expedited review
No
Location
Lone Tree, CO
Statement
Approval for modifications to your device to allow the patient to undergo Magnetic Resonance Imaging (MRI).

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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