# K143337: CONELOG Titanium base CAD/CAM

- Pathway: 510(k) (Traditional)
- Applicant: Altatec GmbH
- Decided: Feb 17, 2015 after 89 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: 13 generations back to K894595 (1990). 195 ancestors in all.
No later device cites it as a predicate yet.
0 of 196 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K133991: ISY, Altatec GmbH (2014) Summary page 5.
- K113779: Conelog Implant System, Altatec GmbH (2012) Summary page 5.
- K083496: Camlog Implant System Modified Implants and Abutments, Altatec GmbH (2009) Summary page 5.
- K111421: Sirona Dental Cad/Cam System, Sirona Dental Systems GmbH (2012) Summary page 5.

## Indications for use
CONELOG® Titanium base CAD/CAM - Implant-prosthetic titanium abutment for CONELOG® implants with conical abutment connection, as a bonding base for hybrid abutments. - The Titanium base CAD/CAM for implant Ø 3.3 mm is designed only for hybrid abutments in the area of the upper lateral incisors and lower central and lateral incisors.

Source page: https://510kreport.com/device/K143337
Methodology: https://510kreport.com/methodology