| Note: this medical device record is a supplement. The device description may have changed. Be sure to look at the original PMA to get an up-to-date view of this device. |
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| Trade Name | ACRYSOF TORIC IOL & ACRYSOF IQ TORIC IOL |
| Classification Name | intraocular lens |
| Generic Name | intraocular lenses (iol)21 cfr 886.3600/class iii |
| Regulation Number | 886.3600 |
| Applicant | ALCON RESEARCH, LTD. |
| PMA Number | P930014 |
| Supplement Number | S045 |
| Date Received | 08/31/2010 |
| Decision Date | 05/03/2011 |
| Product Code | |
| Docket Number | 11M-0338 |
| Notice Date | 05/12/2011 |
| Advisory Committee |
Ophthalmic |
| Clinical Trials |
NCT00967473
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| Supplement Type | panel track |
| Supplement Reason | change design/components/specifications - component |
| Expedited Review Granted? | No |
| Combination Product |
No
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| Information About: |
Labeling, Approval Order, Summary of Safety and Effectiveness |
Approval Order Statement Approval for the acrysof toric posterior chamber intraocular lens models sn60t6, sn60t7, sn60t8, and sn60t9 and acrysof iq toric posterior chamber intraocular lens models sn6at6, sn6at7, sn6at8 and sn6at9. This device is indicated for primary implantation in the capsular bag of the eye for visual correction of aphakia and pre-existing corneal astigmatism secondary to removal of a cataractous lens in adult patients with or without presbyopia, who desire improved uncorrected distance vision, reduction of residual refractive cylinder and increased spectacle independence for distance vision. |
| Approval Order |
Approval Order
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| Post-Approval Study | Show Report Schedule and Study Progress |
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