HiResolution Bionic Ear System
FDA premarket approval P960058/S163 · decided 2024-01-05
Approval details
- PMA number
- P960058
- Supplement
- S163
- Supplement type
- 30-Day Notice
- Supplement reason
- Process Change - Manufacturer/Sterilizer/Packager/Supplier
- Trade name
- HiResolution Bionic Ear System
- Generic name
- Implant, cochlear
- Applicant
- Advanced Bionics
- Date received
- 2023-12-07
- Decision date
- 2024-01-05
- Days to decision
- 29 days
- Decision code
- OK30
- Product code
- MCM
- Advisory committee
- Ear, Nose, Throat
- Expedited review
- No
- Location
- Valencia, CA
- Statement
- an additional supplier for the Printed Circuit Board Assembly (PCBA) used in the the Ultra implants
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