# OCJ: Spinal Channeling Instrument, Vertebroplasty

- Device class: 1; regulation: 21 CFR 888.4540; FDA's rule: 510(k) exempt
- FDA decisions: 1
- Recalls: 2 (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)
- 2007: 1

## Most-cited predicates
- K070293: Benvenue VCF Osteo Coil System (2007), cited by 1

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