# OLC: Scaffold, Partial Medial Meniscal Defects Extending Into The Red/White Zone, Resorbable Bovine Collagen

- Device class: 2; regulation: 21 CFR 878.3300; FDA's rule: 510(k) required
- FDA decisions: 3
- 510(k) review time 2021–2025: median 58 days (middle half 58–58)
- 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)
- 2008: 1
- 2017: 1
- 2024: 1

## Most-cited predicates
- K082079: Regen Collagen Scaffold (CS) (2008), cited by 1
- K170364: Collagen Meniscus Implant XL (2017), cited by 1

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