iSert Preloaded Posterior Chamber One-Piece Intraocular Lens (IOL)
FDA premarket approval P080004/S034 · decided 2020-06-15
Approval details
- PMA number
- P080004
- Supplement
- S034
- Supplement type
- Real-Time Process
- Supplement reason
- Change Design/Components/Specifications/Material
- Trade name
- iSert Preloaded Posterior Chamber One-Piece Intraocular Lens (IOL)
- Generic name
- intraocular lens
- Applicant
- Hoya Surgical Optics, Inc.
- Date received
- 2020-03-18
- Decision date
- 2020-06-15
- Days to decision
- 89 days
- Decision code
- APPR
- Product code
- HQL
- Advisory committee
- Ophthalmic
- Expedited review
- No
- Location
- Chino Hills, CA
- Statement
- Approval for two new IOL models, iSert® models 254 and 255 which are minor modifications of approved parent preloaded IOL iSert® Model 251.
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510(k) clearances by this applicant
| Record | Firm | Date |
|---|---|---|
| HOYA IS INJECTOR SYSTEM (K081346) | Hoya Surgical Optics, Inc. | 2009-03-23 |