# MAJ: Catheter, Percutaneous, Intraspinal, Short Term

- Device class: 2; regulation: 21 CFR 868.5120; FDA's rule: 510(k) required
- FDA decisions: 6
- Recalls: 0 (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)
- 1989: 1
- 1991: 1
- 1993: 1
- 1995: 2
- 1997: 1

## Most-cited predicates
- K893766: Lifecare Cont. Epidural Cath. for Morphine Sulfate (1989), cited by 1

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