Atlas FDA

GLAUKOS CORPORATION ISTENT TRABECULAR MICRO-BYPASS STENT SYSTEM

FDA premarket approval P080030/S006 · decided 2012-09-18

Approval details

PMA number
P080030
Supplement
S006
Supplement type
30-Day Notice
Supplement reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Trade name
GLAUKOS CORPORATION ISTENT TRABECULAR MICRO-BYPASS STENT SYSTEM
Generic name
Intraocular pressure lowering implant
Applicant
Glaukos Corporation
Date received
2012-08-21
Decision date
2012-09-18
Days to decision
28 days
Decision code
OK30
Product code
OGO
Advisory committee
Ophthalmic
Expedited review
No
Location
Laguna Hills, CA
Statement
ADDITION OF A SECOND CLEAN ROOM AND TO PERFORM IN HOUSE PEEL TESTING.

Class III intelligence, same tools

PMAs share the API, exports and alerts with 510(k) data - watch an applicant and hear about every approval.

510(k) clearances by this applicant

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