Atlas FDA

iStent inject Trabecular Micro-Bypass System

FDA premarket approval P170043/S008 · decided 2021-03-03

Approval details

PMA number
P170043
Supplement
S008
Supplement type
Normal 180 Day Track No User Fee
Supplement reason
Postapproval Study Protocol
Trade name
iStent inject Trabecular Micro-Bypass System
Generic name
Intraocular pressure lowering implant
Applicant
Glaukos Corporation
Date received
2020-12-07
Decision date
2021-03-03
Days to decision
86 days
Decision code
APPR
Product code
OGO
Advisory committee
Ophthalmic
Expedited review
No
Location
San Clemente, CA
Statement
Approval of the revised PAS protocol, IG2M-105-PASN to include the modified device version, Model G2-W

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510(k) clearances by this applicant

RecordFirmDate
iStent infinite Trabecular Micro-Bypass System, Model iS3 (K220032)Glaukos Corporation2022-08-02