# K152509: CAMLOG and CONELOG Abutments for Screw-retained Restorations (ASR)

- Pathway: 510(k) (Traditional)
- Applicant: Altatec GmbH
- Decided: Jan 12, 2016 after 132 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: 11 generations back to K894595 (1990). 72 ancestors in all.
No later device cites it as a predicate yet.
0 of 73 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K133421: Straumann Magellan (TM) Abutment,Protective Cap,Titanium Copings,Gold Chopings,Basal Screw, Straumann USA, LLC (2014) Summary page 5.
- K141871: Straumann Bone Level NC Angled Screw Retained Abutments, Straumann USA, LLC (2014) Summary page 5.

## Indications for use
CAMLOG® and CONELOG® Abutments for Screw-retained Restorations (ASR) are intended to support occlusal screw-retained prosthetic restorations in the upper jaw and lower jaw in conjunction with CAMLOG® and CONELOG® Implants.

Source page: https://510kreport.com/device/K152509
Methodology: https://510kreport.com/methodology