FDA PMA FDA Class 3 Approved 🇺🇸 United States

Intraocular Pressure Lowering Implant

PMA: P170043 · Supplement: S007 · Decision Apr 30, 2020
Classifications
1
FEI Numbers
9
Registration Numbers
9

Basic Information

Device Name
Intraocular Pressure Lowering Implant
Trade Name
iStent inject Trabecular Micro-Bypass System
PMA Number
P170043
Supplement Number
S007
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
April 30, 2020
Date Received
March 3, 2020
Supplement Type
Normal 180 Day Track No User Fee
Supplement Reason
Postapproval Study Protocol
Expedited Review
N

Advisory Committee Statement

Approval of the revised protocol for the post-approval study (PAS) protocol.

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