TECHNOLAS 217A EXCIMER LASER SYSTEM FOR LASER IN-SITU KERATOMILEUSIS(LASIK), TECHNOLAS 217Z ZYOPTIX SYSTEM FOR PERSONALI
FDA premarket approval P990027/S020 · decided 2015-11-05
Approval details
- PMA number
- P990027
- Supplement
- S020
- Supplement type
- 30-Day Notice
- Supplement reason
- Process Change - Manufacturer/Sterilizer/Packager/Supplier
- Trade name
- TECHNOLAS 217A EXCIMER LASER SYSTEM FOR LASER IN-SITU KERATOMILEUSIS(LASIK), TECHNOLAS 217Z ZYOPTIX SYSTEM FOR PERSONALI
- Generic name
- Excimer laser system
- Applicant
- Technolas Perfect Vision GmbH
- Date received
- 2015-10-07
- Decision date
- 2015-11-05
- Days to decision
- 29 days
- Decision code
- OK30
- Product code
- LZS
- Advisory committee
- Ophthalmic
- Expedited review
- No
- Location
- München
- Statement
- THE REPLACEMENT OF THE SUPPLIER OF ONE COMPONENT OF YOUR TREATMENT CARD BY TWO OTHER SUPPLIERS.
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510(k) clearances by this applicant
| Record | Firm | Date |
|---|---|---|
| VICTUS Femtosecond Laser Platform (K200724) | Technolas Perfect Vision GmbH | 2020-09-01 |
| VICTUS Femtosecond Laser Platform (K171014) | Technolas Perfect Vision GmbH | 2017-10-19 |
| VICTUS Femtosecond Laser Platform (K151161) | Technolas Perfect Vision GmbH | 2015-06-24 |
| VICTUS FEMTOSECOND LASER PLATFORM (K141379) | Technolas Perfect Vision GmbH | 2015-01-16 |
| VICTUS FEMTOSECOND LASER PLATFORM (K140615) | Technolas Perfect Vision GmbH | 2014-07-15 |
| VICTUS FEMTOSECOND LASER PLATFORM (K132534) | Technolas Perfect Vision GmbH | 2014-02-14 |
| VICTUS FEMTOSECOND LASER PLATFORM (K122386) | Technolas Perfect Vision GmbH | 2013-02-08 |
| VICTUS LASER PLATFORM (K120426) | Technolas Perfect Vision GmbH | 2012-07-31 |