FDA PMA FDA Class 3 Approved 🇺🇸 United States

Intraocular Pressure Lowering Implant

PMA: P170043 · Supplement: S005 · Decision Jul 2, 2020
Classifications
1
FEI Numbers
9
Registration Numbers
9

Basic Information

Device Name
Intraocular Pressure Lowering Implant
Trade Name
iStent inject W Trabecular Micro-Bypass System
PMA Number
P170043
Supplement Number
S005
Device Class
FDA Class 3
Product Code
OGO
Generic Name
Intraocular pressure lowering implant
Medical Specialty
Unknown
Advisory Committee
Ophthalmic
Decision
Approved
Decision Code
APPR
Decision Date
July 2, 2020
Date Received
November 29, 2019
Supplement Type
Normal 180 Day Track
Supplement Reason
Change Design/Components/Specifications/Material
Expedited Review
N

Advisory Committee Statement

Approval for design changes to the stent implant and injector.

Classifications

This FDA Pre-Market Approval entry is associated with 1 FDA classification via its product code.

Product Code Device Name
OGO Intraocular Pressure Lowering Implant