# K862061: Osteograf/AR+ Permaridge Hydroxylapatite, 18-40

- Pathway: 510(k) (Traditional)
- Applicant: Coors Biomedical Co.
- Decided: Jul 29, 1986 after 60 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
No predicates in its family tree.
33 later devices descend from it; 2 cite it directly.
0 of 34 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
- K073070: Dio Biotite-H Implant System (2008), 16 descendants of its own
- K030682: Calcium Hydroxylapatite Implant, Icc and 0.5CC, Models 8038-3, 8037-3 (2003), 15 descendants of its own
- K112532: ET II Bio-SA Fixture System (2012), 10 descendants of its own
- K033398: Laryngeal Augmentation Implant (2003), 10 descendants of its own
- K151626: ET III Bio-SA Fixture System (2016), 9 descendants of its own

Source page: https://510kreport.com/device/K862061
Methodology: https://510kreport.com/methodology