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. |
|
Device | PROVISC OPHTHALMIC VISCOSURGICAL DEVICE |
Generic Name | AID, SURGICAL, VISCOELASTIC |
Regulation Number | 886.4275 |
Applicant | Alcon Research, Ltd. 6201 SOUTH FREEWAY, R3-48 FORT WORTH, TX 76134-2099 |
PMA Number | P890047 |
Supplement Number | S042 |
Date Received | 08/16/2013 |
Decision Date | 11/13/2013 |
Product Code |
LZP |
Advisory Committee |
Ophthalmic |
Supplement Type | Normal 180 Day Track |
Supplement Reason | Change Design/Components/Specifications/Material |
Expedited Review Granted? | No |
Combination Product | No |
Approval Order Statement APPROVAL TO DISCONTINUE THE CURRENT INTRAVITREAL TEST AND REPLACE IT WITH THE INFLAMMATORY RELEASE ASSAY FOR THE PROVISC IBC OPHTHALMIC VISCOSURGICAL DEVICE. |
|
|