# K151161: VICTUS Femtosecond Laser Platform

- Pathway: 510(k) (Traditional)
- Applicant: Technolas Perfect Vision GmbH
- Decided: Jun 24, 2015 after 54 days
- Product code: OOE (Ophthalmic Femtosecond Laser)
- Device class: 2
- Regulation: 21 CFR 886.4390
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 16 generations back to K913697 (1991). 91 ancestors in all.
2 later devices descend from it; 1 cites it directly.
0 of 94 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K132534: Victus Femtosecond Laser Platform, Technolas Perfect Vision GmbH (2014) Summary page 4.
- K141379: Victus Femtosecond Laser Platform, Technolas Perfect Vision GmbH (2015) Summary page 4.
- K140615: Victus Femtosecond Laser Platform, Technolas Perfect Vision GmbH (2014) Summary page 4.

## Most influential descendants
- K171014: VICTUS Femtosecond Laser Platform (2017), 1 descendant of its own
- K200724: VICTUS Femtosecond Laser Platform (2020), 0 descendants of its own

## Indications for use
The VICTUS Femtosecond Laser Platform is indicated for use for: • the creation of a corneal flap in patients undergoing LASIK surgery or other treatment requiring initial lamellar resection of the cornea. • for anterior capsulotomy during cataract surgery. • the creation of cuts / incisions in the cornea in patients undergoing cataract surgery or other ophthalmic treatment. • laser-assisted lens fragmentation of nuclear cataracts during cataract surgery, not for fragmentation of posterior subcapsular (PSC) and cortical cataracts

Source page: https://510kreport.com/device/K151161
Methodology: https://510kreport.com/methodology