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U.S. Department of Health and Human Services

Premarket Approval (PMA)

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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.
 
DeviceACRYSOF TORIC POSTERIOR CHAMBER INTRAOCULAR LENS MODELS SA60T3, SA60T4 AND SA60T5
Classification Nameintraocular lens
Generic Nameintraocular lens
Regulation Number886.3600
Applicant
Alcon Research, Ltd.
6201 south freeway dr.
fort worth, TX 76134
PMA NumberP930014
Supplement NumberS015
Date Received03/18/2005
Decision Date09/14/2005
Product Code
HQL[ Registered Establishments with HQL ]
Docket Number 05M-0378
Notice Date 09/23/2005
Advisory Committee Ophthalmic
Supplement Typepanel track
Supplement Reason labeling change - indications/instructions/shelf life/tradename
Expedited Review Granted? No
Combination Product No
Approval Order Statement 
Approval for the acrysof toric posterior chamber intraocular lens models sa60t3, sa60t4 and sa60t5. The devices are 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
Summary Summary of Safety and Effectiveness
Labeling Labeling
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