# K852682: Calcitite Bone Graft Mat/Oral & Maxillofacial Surg

- Pathway: 510(k) (Traditional)
- Applicant: Calcitek, Inc.
- Decided: Sep 23, 1985 after 90 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.
190 later devices descend from it; 2 cite it directly.
0 of 191 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
- K992416: Perioglas- Bioglass Bone Graft Particulate (1999), 189 descendants of its own
- K033994: Novabone-BBG-Resorbable Bone Graft Substitute (2004), 85 descendants of its own
- K041613: Novabone - AR - Resorbable Bone Graft Substitute (2004), 84 descendants of its own
- K040278: Perioglas-Bioglass Bone Graft Substitute (2004), 80 descendants of its own
- K082672: Novabone Putty-Bioactive Synthetic Bone Graft (2008), 59 descendants of its own

Source page: https://510kreport.com/device/K852682
Methodology: https://510kreport.com/methodology