Atlas FDA

Hydrus Microstent

FDA premarket approval P170034/S004 · decided 2020-01-23

Approval details

PMA number
P170034
Supplement
S004
Supplement type
Normal 180 Day Track No User Fee
Supplement reason
Postapproval Study Protocol
Trade name
Hydrus Microstent
Generic name
Intraocular pressure lowering implant
Applicant
Alcon Research, LLC
Date received
2019-11-27
Decision date
2020-01-23
Days to decision
57 days
Decision code
APPR
Product code
OGO
Advisory committee
Ophthalmic
Expedited review
No
Location
Fort Worth, TX
Statement
Approval of the revised protocol for the post-approval study (PAS) protocol.

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510(k) clearances by this applicant

RecordFirmDate
LEGION System (K191650)Alcon Research, LLC2019-11-01