# K924112: Hydroxylapatite Coated Saber Tech Series I & Series II

- Pathway: 510(k) (Traditional)
- Applicant: Saber Technology, Inc.
- Decided: Jul 12, 1994 after 718 days
- Product code: DZE (Implant, Endosseous, Root-Form)
- Device class: 2
- Regulation: 21 CFR 872.3640
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
5 later devices descend from it; 3 cite it directly.
0 of 6 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
- K991250: Quantum Versatility Implant System (2001), 2 descendants of its own
- K112279: Quantum Dental Implant System (2012), 1 descendant of its own
- K980442: Crystal and Crystal-Seal Implants System (1998), 1 descendant of its own
- K130787: Quantum Dental Implant System (2013), 0 descendants of its own
- K034067: Zti Implants System, DRM Implants (2004), 0 descendants of its own

Source page: https://510kreport.com/device/K924112
Methodology: https://510kreport.com/methodology