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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.
 
Trade NameSOFTEC HD POSTERIOR CHAMBER INTRAOCULAR LENS (PCIOL)
Classification Nameintraocular lens
Regulation Number886.3600
ApplicantLENSTEC, INC.
PMA NumberP090022
Supplement NumberS011
Date Received03/14/2012
Decision Date06/11/2012
Product Code
HQL[ Registered Establishments with HQL ]
Advisory Committee Ophthalmic
Supplement Typereal-time process
Supplement Reason change design/components/specifications - component
Expedited Review Granted? No
Combination Product No
Approval Order Statement 
Approval for modifications to the optic body shape and overall diameter of your softec hd lens to introduce a lens with an ovoid optic and overall diameter of 12. 50 mm and changes to your labeling related to the introduction of the modified lens. The device, as modified, will be marketed under the trade name softec hdo and is indicated for the replacement of the human crystalline lens following phacoemulsifica- tion cataract removal in adults over the age of 21. The lens is indicated for capsular bag placement.
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