# K051486: Norwood Abbey Centurion Ses  Epikeratome

- Pathway: 510(k) (Special)
- Applicant: Norwood Abbey, Ltd.
- Decided: Jul 6, 2005 after 30 days
- Product code: HNO (Keratome, Ac-Powered)
- Device class: 1
- Regulation: 21 CFR 886.4370
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
1 later device descends from it; 1 cites it directly.
0 of 2 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. The FDA summary names its predicate without a number.
- (no number) Centurion SES Epikeratome: named in the summary without a submission number

## Most influential descendants
- K052891: Horizon Epikeratome Disposable Microkeratome System (2006), 0 descendants of its own

## Indications for use
The Norwood Abbey Centurion SES Epikeratome is intended for use in the separation of the epithelium from the cornea in preparation for subsequent surgical procedures on the denuded cornea.

Source page: https://510kreport.com/device/K051486
Methodology: https://510kreport.com/methodology