# SBG: In Situ Polymerizing Peripheral Nerve Cap

- Device class: 2; regulation: 21 CFR 882.5260; FDA's rule: 510(k) required
- FDA decisions: 2
- 510(k) review time 2021–2025: median 90 days (middle half 90–90)
- 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)
- 2024: 1
- 2025: 1

## Most-cited predicates
- DEN230061: allay Nerve Cap (2024), cited by 1

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