# K033390: Colibri Disposable Vitrectomy Cutter

- Pathway: 510(k) (Traditional)
- Applicant: Microworld Medical Instruments, Inc.
- Decided: Nov 4, 2003 after 12 days
- Product code: HQE (Instrument, Vitreous Aspiration And Cutting, Ac-Powered)
- Device class: 2
- Regulation: 21 CFR 886.4150
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
No later device cites it as a predicate yet.
0 of 1 device 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) Bausch & Lomb Surgical MicroVitO Vitrectomy Cutter: named in the summary without a submission number
- (no number) M. lmonti and Associates Pro-Vit Vitrectomy Cutter: named in the summary without a submission number
- (no number) D.O.R.C. Disposable Pneumatic Vitrectome: named in the summary without a submission number

## Indications for use
The COLlBRl Disposable Vitrectomy Cutter is intended to be used for the removal of vitreous and vitreal membranes during ophthalmic surgery.

Source page: https://510kreport.com/device/K033390
Methodology: https://510kreport.com/methodology