# K072056: Osteograf/D-700

- Pathway: 510(k) (Special)
- Applicant: Dentsply International, Inc.
- Decided: Aug 6, 2007 after 11 days
- Product code: LYC (Bone Grafting Material, Synthetic)
- Device class: 2
- Regulation: 21 CFR 872.3930
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 1 generation back to K852742 (1985). 4 ancestors in all.
2 later devices descend from it; 1 cites it directly.
0 of 7 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K863176: Additional Clinical Usages for Osteograf/AR & AR+, Coors Biomedical Co. (1986) Summary page 1.
- K861084: Osteograf/AR Alveolar Rid Hydrox, 18-40 Mesh, Coors Biomedical Co. (1986) Summary page 1.
- K861083: Osteograf/AR+(Plus) Alveolar Rid Hydrox 18-40 Mesh, Coors Biomedical Co. (1986) Summary page 1.
- K852742: Osteograf AR Alveolar Ridge Hydroxylapatite 18-40, Coors Biomedical Co. (1985) Summary page 1.

## Cited in the summary but kept off the family tree
- K863234: OsteoGraf/D-700. Not in FDA’s 510(k), De Novo or PMA lists as we hold them (a misreading, a typo, or a number FDA does not list), so it is kept off the family tree Summary page 1.

## Most influential descendants
- K102872: Osbone Dental (2011), 1 descendant of its own
- K202675: InRoad® Dental Synthetic Bone Graft (2022), 0 descendants of its own

## Indications for use
OsteoGraf/D-700 is indicated for treatment of intrabony periodontal defects, augmentation of bony defects in the alveolar ridge, and filing of extraction sites. These are the same indications for use previously cleared for K852742, K863176, and K862324.

Source page: https://510kreport.com/device/K072056
Methodology: https://510kreport.com/methodology