NUCLEUS 24 HYBRID SYSTEM
FDA premarket approval P130016/S013 · decided 2015-12-30
Approval details
- PMA number
- P130016
- Supplement
- S013
- Supplement type
- 30-Day Notice
- Supplement reason
- Process Change - Manufacturer/Sterilizer/Packager/Supplier
- Trade name
- NUCLEUS 24 HYBRID SYSTEM
- Generic name
- Cochlear implant with combined electrical stimulation and acoustic amplification
- Applicant
- Cochlear Americas
- Date received
- 2015-12-04
- Decision date
- 2015-12-30
- Days to decision
- 26 days
- Decision code
- OK30
- Product code
- PGQ
- Advisory committee
- Ear, Nose, Throat
- Expedited review
- No
- Location
- Lone Tree, CO
- Statement
- APPROVAL FOR A CHANGE TO THE PRE-STERILIZATION CLEANING PROCESS TO ALLOW FOR ADDITIONAL DEVICES TO BE CLEANED PRIOR TO THE STERILIZATION CYCLE.
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