# K090871: Cerament Ibone Void Filler High Contrast, Model a 0210-12

- Pathway: 510(k) (Traditional)
- Applicant: Bonesupport AB
- Decided: Sep 4, 2009 after 158 days
- Product code: MQV (Filler, Bone Void, Calcium Compound)
- Device class: 2
- Regulation: 21 CFR 888.3045
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 6 generations back to K960978 (1996). 14 ancestors in all.
1 later device descends from it; 1 cites it directly.
0 of 16 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K073316: Cerament Bone Void Filler, Model A0210, Bonesupport AB (2008) Summary page 1.

## Most influential descendants
- K121177: Bond Apatite (2013), 0 descendants of its own

## Indications for use
CERAMENTTMIBONE VOID FILLER is a ceramic bone void filler intended only for orthopedic applications as a filler for gaps and voids that are not intrinsic to the stability of the bony structure. CERAMENTTMJBONE VOID FILLER is indicated to be injected into bony voids or gaps in the skeletal system, i.e. extremities, pelvis and spine (only during open surgery in spine). These defects may be surgically created osseous defects or osseous defects from traumatic injury to the bone. CERAMENT MJBONE VOID FILLER provides a bone void filler that resorbs and is replaced by bone during the healing process.

Source page: https://510kreport.com/device/K090871
Methodology: https://510kreport.com/methodology