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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 PMA supplement. A supplement may have changed the device description/function or indication from that approved in the original PMA. Be sure to look at the original PMA record for more information.
 
DeviceKAMRA INLAY
Generic NameImplant, corneal, refractive
ApplicantCorneaGen
1200 6th Avenue
Suite 300
Seattle, WA 98101
PMA NumberP120023
Supplement NumberS001
Date Received05/18/2015
Decision Date05/12/2016
Withdrawal Date 02/03/2022
Product Code LQE 
Advisory Committee Ophthalmic
Supplement TypeNormal 180 Day Track No User Fee
Supplement Reason Postapproval Study Protocol - OSB
Expedited Review Granted? No
Combination ProductNo
Approval Order Statement  
Approval of the post approval study protocol.
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