# K950165: Interpore IP 200 Granular Coralline Hydroxyapatite Bone Void Fillers, 425 to 1000 Microns and 425 to 600 Microns

- Pathway: 510(k) (Traditional)
- Applicant: Interpore Intl.
- Decided: Mar 28, 1995 after 70 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.
2 later devices descend from it; 2 cite it directly.
0 of 3 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA lists a 510(k) statement for it but has not posted the file, so its predicates are not known.

## Most influential descendants
- K023799: Frios Algipore (2003), 1 descendant of its own
- K033110: C-Graft (2003), 0 descendants of its own

Source page: https://510kreport.com/device/K950165
Methodology: https://510kreport.com/methodology