# MBS: Filler, Bone Void, Non-Osteoinduction

- Device class: 3; regulation: 21 CFR —; FDA's rule: PMA required
- FDA decisions: 2
- 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)
- 1993: 4
- 1994: 5
- 1995: 3
- 1996: 2
- 1997: 2
- 1998: 4
- 1999: 1
- 2002: 3
- 2004: 1
- 2005: 1

## Most-cited predicates

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