# K000122: Collagraft Strip Bone Graft Matrix (for Use as a Bone Filler), Model 1X,3X,6X (1,3 or 6 Strips Per Box)

- Pathway: 510(k) (Traditional)
- Applicant: Neucoll, Inc.
- Decided: Sep 20, 2001 after 611 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.
253 later devices descend from it; 7 cite it directly.
0 of 254 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
- K012751: Healos Bone Graft Material (2001), 84 descendants of its own
- K080009: Novabone Putty- Bioactive Synthetic Graft (2008), 71 descendants of its own
- K043308: Modification to: Healos Bone Graft Material (2005), 67 descendants of its own

Source page: https://510kreport.com/device/K000122
Methodology: https://510kreport.com/methodology