# Bonesupport AB

- Location (FDA's records): Lund, SE
- FDA decisions: 7 (2005–2024): 6 510(k) clearances and 1 De Novo grant
- Product codes: MQV (5), QRR (2)
- Predicates its devices cite: 12 (4 its own); citations of its devices by later devices: 8 (4 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Wrightmedicaltechnologyinc: 2 (https://510kreport.com/company/wrightmedicaltechnologyinc)
- Berkeley Advanced Biomaterials, Inc.: 1 (https://510kreport.com/company/berkeley-advanced-biomaterials)
- Synthes (Usa): 1 (https://510kreport.com/company/synthes-usa)
- Apatech, Ltd.: 1 (https://510kreport.com/company/apatech)
- Lifecore Biomedical, Inc.: 1 (https://510kreport.com/company/lifecore-biomedical)
- Nu Vasive, Incorporated: 1 (https://510kreport.com/company/nu-vasive)
- Depuy Spine, Inc.: 1 (https://510kreport.com/company/depuy-spine)

## Firms that cite its devices most
- Anika Therapeutics, Inc.: 2 (https://510kreport.com/company/anika-therapeutics)
- Bone Solutions, Inc.: 1 (https://510kreport.com/company/bone-solutions)
- Augma Biomaterials, Ltd.: 1 (https://510kreport.com/company/augma-biomaterials)

## Its most-cited devices
- K051951: Cerament Bone Void Filler (2005), cited by 2
- K073316: Cerament Bone Void Filler, Model A0210 (2008), cited by 2
- K201535: Cerament Bone Void Filler (2020), cited by 2
- K090871: Cerament Ibone Void Filler High Contrast, Model a 0210-12 (2009), cited by 1
- DEN210044: Cerament G (2022), cited by 1

## Recent decisions
- K234008: Cerament G (Mar 13, 2024)
- K240459: Cerament Bone Void Filler (Mar 5, 2024)
- DEN210044: Cerament G (May 17, 2022)
- K201535: Cerament Bone Void Filler (Oct 16, 2020)
- K090871: Cerament Ibone Void Filler High Contrast, Model a 0210-12 (Sep 4, 2009)
- K073316: Cerament Bone Void Filler, Model A0210 (Jun 20, 2008)
- K051951: Cerament Bone Void Filler (Sep 28, 2005)

Source page: https://510kreport.com/company/bonesupport