# LRN: Wire, Surgical

- Device class: 2; regulation: 21 CFR 888.3030; FDA's rule: 510(k) required
- FDA decisions: 8
- Recalls: 1 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026; MAUDE to Sep 30, 2026

## Decisions per year (last 10)
- 1987: 1
- 1989: 1
- 1990: 1
- 1994: 1
- 1995: 1
- 1997: 1
- 1999: 1
- 2000: 1

## Most-cited predicates
- K900926: Trochanter Cable Grip System (Add'l Indications) (1990), cited by 9
- K971682: J-FX Cerclage System (1997), cited by 2

Source page: https://510kreport.com/product-code/LRN
Data by year (CSV): https://510kreport.com/product-code/LRN.csv