# P860005: Pro Osteon Implant 500 Hydroxyapatite Bone Void Filler

- Pathway: PMA
- Applicant: Interpore Intl.
- Decided: Oct 29, 1992 after 2,453 days
- Product code: OIS (Calcium Salt Bone Void Filler, Drillable, Non-Screw Augmentation)
- 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.
1 later device descends from it; 1 cites it directly.
0 of 2 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. PMA decisions do not claim a predicate device.

## Most influential descendants
- K070897: Bonemedik, and Bonemedik-S (2007), 0 descendants of its own

Source page: https://510kreport.com/device/P860005
Methodology: https://510kreport.com/methodology