Nucleus Hybrid L24 Implant System
FDA premarket approval P130016/S023 · decided 2017-03-29
Approval details
- PMA number
- P130016
- Supplement
- S023
- Supplement type
- 30-Day Notice
- Supplement reason
- Process Change - Manufacturer/Sterilizer/Packager/Supplier
- Trade name
- Nucleus Hybrid L24 Implant System
- Generic name
- Cochlear implant with combined electrical stimulation and acoustic amplification
- Applicant
- Cochlear Americas
- Date received
- 2017-02-27
- Decision date
- 2017-03-29
- Days to decision
- 30 days
- Decision code
- OK30
- Product code
- PGQ
- Advisory committee
- Ear, Nose, Throat
- Expedited review
- No
- Location
- Lone Tree, CO
- Statement
- Manufacturing change to the CP950 Sound Processor.
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