iStent inject Trabecular Micro-Bypass System (Model G2-M-IS)
FDA premarket approval P170043/S004 · decided 2019-05-30
Approval details
- PMA number
- P170043
- Supplement
- S004
- Supplement type
- 30-Day Notice
- Supplement reason
- Process Change - Manufacturer/Sterilizer/Packager/Supplier
- Trade name
- iStent inject Trabecular Micro-Bypass System (Model G2-M-IS)
- Generic name
- Intraocular pressure lowering implant
- Applicant
- Glaukos Corporation
- Date received
- 2019-05-02
- Decision date
- 2019-05-30
- Days to decision
- 28 days
- Decision code
- OK30
- Product code
- OGO
- Advisory committee
- Ophthalmic
- Expedited review
- No
- Location
- San Clemente, CA
- Statement
- Modification to the endotoxin specification for the injector handpiece for the Glaukos® iStent inject® Trabecular Micro-Bypass System (Model G2-M-IS).
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510(k) clearances by this applicant
| Record | Firm | Date |
|---|---|---|
| iStent infinite Trabecular Micro-Bypass System, Model iS3 (K220032) | Glaukos Corporation | 2022-08-02 |