Intraocular Lens
Basic Information
- Device Name
- Intraocular Lens
- Trade Name
- ANTERIOR CHAMBER INTRAOCULAR LENS (CATARACT)
- PMA Number
- P010027
- Device Class
- FDA Class 3
- Product Code
- HQL
- Generic Name
- intraocular lens
- Regulation Number
- 886.3600
- Medical Specialty
- Ophthalmic
- Advisory Committee
- Ophthalmic
- Decision
- Approved (Withdrawn)
- Decision Code
- APWD
- Decision Date
- November 21, 2001
- Date Received
- April 30, 2001
- Expedited Review
- N
- Docket Number
- 02M-0180
Advisory Committee Statement
APPROVAL FOR THE ALLERGAN, INC. MODEL AC21B ULTRAVIOLET-ABSORBING PMMA ANTERIOR CHAMBER INTRAOCULAR LENS, AVAILABLE IN THREE OVERALL DIAMETERS (12.0 MM, 13.0 MM, 14.0 MM). THE APPLICATION IS A LICENSING PMA IN WHICH ALLERGAN, INC. HAS GIVING OPHTHALMIC INNOVATIONS INTERNATIONAL, INC. REFERENCE RIGHTS TO P860034. ADDITIONALLY, IT IS REQUESTED THAT ALLERGAN, INC. DISTRIBUTE THE LENS AS THE DURALENS II MODEL AC21B. THE DEVICE IS INDICATED FOR THE REPLACEMENT OF THE HUMAN LENS IN THE VISUAL CORRECTION OF APHAKIA. THE ANTERIOR CHAMBER INTRAOCULAR LENS IS TO BE USED IN PATIENTS 60 YEARS OF AGE AND OLDER WHERE A CATARACTOUS LENS HAS BEEN REMOVED BY PRIMARY INTRACAPSULAR CATARACT EXTRACTION (ICCE); OR BY PRIMARY EXTRACAPSULAR CATARACT EXTRACTION (ECCE) WHERE THERE IS A STRUCTURAL REASON THAT THE ANTERIOR CHAMBER LENS IS THE PREFERRED ONE; OR OTHER PRIMARY ECCE PROVIDED THAT THIS BE PERFORMED ONLY AFTER THE PHYSICIAN HAS COMPARED THE PUBLISHED RESULTS OF THE ANTERIOR CHAMBER LENS WITH POSTERIOR CHAMBER LENSES; OR IN A SECONDARY IMPLANT PROCEDURE.
Classifications
This FDA Pre-Market Approval entry is associated with 1 FDA classification via its product code.
| Product Code | Device Name | Device Class | Medical Specialty |
|---|---|---|---|
| HQL | Intraocular Lens | FDA class 3 | Ophthalmic |