# K011386: Ebi Osteostim Granules-Resorbable Bone Graft Substitute

- Pathway: 510(k) (Traditional)
- Applicant: Ebi, L.P.
- Decided: Aug 3, 2001 after 88 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
No predicates in its family tree.
188 later devices descend from it; 2 cite it directly.
0 of 189 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA has not posted a summary or statement for it, so its predicates are not known.

## Most influential descendants
- K020078: Exactech Resorbable Bone Paste (2004), 186 descendants of its own
- K060728: Novabone Putty - Bioactive Synthetic Graft (2006), 120 descendants of its own
- K080009: Novabone Putty- Bioactive Synthetic Graft (2008), 71 descendants of its own
- K082672: Novabone Putty-Bioactive Synthetic Bone Graft (2008), 59 descendants of its own
- K072184: Vitoss Bioactive Foam Bone Graft Substitute (2007), 51 descendants of its own

Source page: https://510kreport.com/device/K011386
Methodology: https://510kreport.com/methodology