# K925761: Branemark System 5.0 X 14MM Fixture

- Pathway: 510(k) (Traditional)
- Applicant: Nobelpharma USA, Inc.
- Decided: Oct 5, 1993 after 326 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.
4 later devices descend from it; 1 cites it directly.
0 of 5 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
- K112787: Kerator (2012), 3 descendants of its own
- K241183: ISO Abutment (2025), 0 descendants of its own
- K173141: CSM Submerged3-L Implant System (2018), 0 descendants of its own
- K132144: Kerator (2014), 0 descendants of its own

Source page: https://510kreport.com/device/K925761
Methodology: https://510kreport.com/methodology