# K860983: Interpore 200 Porous Hydroxyapatite

- Pathway: 510(k) (Traditional)
- Applicant: Interpore Intl.
- Decided: May 23, 1986 after 67 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.
11 later devices descend from it; 4 cite it directly.
0 of 12 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
- K042706: Ossatura Dental (2004), 6 descendants of its own
- K082419: Reoss Powder, Reoss Putty, Reoss Gel, Models R-1,RP-1, RG-1 (2009), 2 descendants of its own
- K101827: Osteoscaf (2011), 1 descendant of its own
- K031813: Ossatura Dental (2004), 1 descendant of its own
- K982562: Bio-Eye Hydroxyapatite Ocular Impland and Conformer (1998), 1 descendant of its own

Source page: https://510kreport.com/device/K860983
Methodology: https://510kreport.com/methodology