Cochlear Slimline Coil, Cochlear Slimline Coil (5(I)), Nucleus® 7 Aqua+ Coil (5(I)), Nucleus 7 Aqua+ Coil
FDA premarket approval P970051/S230 · decided 2024-10-25
Approval details
- PMA number
- P970051
- Supplement
- S230
- Supplement type
- 30-Day Notice
- Supplement reason
- Process Change - Manufacturer/Sterilizer/Packager/Supplier
- Trade name
- Cochlear Slimline Coil, Cochlear Slimline Coil (5(I)), Nucleus® 7 Aqua+ Coil (5(I)), Nucleus 7 Aqua+ Coil
- Generic name
- Implant, cochlear
- Applicant
- Cochlear Americas
- Date received
- 2024-09-27
- Decision date
- 2024-10-25
- Days to decision
- 28 days
- Decision code
- OK30
- Product code
- MCM
- Advisory committee
- Ear, Nose, Throat
- Expedited review
- No
- Location
- Lone Tree, CO
- Statement
- approval for manufacturing changes to the CP1000 sound processor coil
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