Clareon Intraocular Lenses with the AutonoMe Delivery System
FDA premarket approval P190018/S007 · decided 2020-11-12
Approval details
- PMA number
- P190018
- Supplement
- S007
- Supplement type
- 30-Day Notice
- Supplement reason
- Process Change - Manufacturer/Sterilizer/Packager/Supplier
- Trade name
- Clareon Intraocular Lenses with the AutonoMe Delivery System
- Generic name
- intraocular lens
- Applicant
- Alcon Laboratories, LLC
- Date received
- 2020-10-16
- Decision date
- 2020-11-12
- Days to decision
- 27 days
- Decision code
- OK30
- Product code
- HQL
- Advisory committee
- Ophthalmic
- Expedited review
- No
- Location
- Fort Worth, TX
- Statement
- Adding an alternate supplier for the hydrophilic monomer used for the manufacturing of the Clareon Intraocular Lens (IOL) in the Alcon Ireland manufacturing site.
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