# K001760: Radiolucent Colles Fracture Kit

- Pathway: 510(k) (Abbreviated)
- Applicant: Biomet, Inc.
- Decided: Aug 31, 2000 after 83 days
- Product code: LXT (Appliance, Fixation, Nail/Blade/Plate Combination, Multiple Component, Metal Composite)
- Device class: 2
- Regulation: 21 CFR 888.3030
- 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. FDA has not posted a summary or statement for it, so its predicates are not known.

## Most influential descendants
- K021182: Radiolucent Colles Compression/Distraction Bar (2002), 0 descendants of its own

Source page: https://510kreport.com/device/K001760
Methodology: https://510kreport.com/methodology