# K153779: Abutment for Bridges

- Pathway: 510(k) (Traditional)
- Applicant: Altatec GmbH
- Decided: Mar 31, 2016 after 91 days
- Product code: NHA (Abutment, Implant, Dental, Endosseous)
- Device class: 2
- Regulation: 21 CFR 872.3630
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 10 generations back to K925765 (1993). 127 ancestors in all.
1 later device descends from it; 1 cites it directly.
0 of 129 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K113779: Conelog Implant System, Altatec GmbH (2012) Summary page 5.
- K083496: Camlog Implant System Modified Implants and Abutments, Altatec GmbH (2009) Summary page 5.

## Most influential descendants
- K231566: ICX-Implant System (2024), 0 descendants of its own

## Indications for use
CAMLOG® and CONELOG® CAMLOG® and CONELOG® Abutments are intended to be used to fabricate prosthetic restorations in conjunction with CAMLOG® and CONELOG® implants to support prostheses in the maxillary and/or mandibular arch. iSy® iSy® Abutments are intended to be used to fabricate prosthetic restorations in conjunction with iSy® implants to support prostheses in the maxillary and/or mandibular arch.

Source page: https://510kreport.com/device/K153779
Methodology: https://510kreport.com/methodology