# K130183: Sfi Bar Abutments

- Pathway: 510(k) (Abbreviated)
- Applicant: Sterngold Dental, LLC
- Decided: Jul 7, 2013 after 163 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: 2 generations back to K083876 (2010). 2 ancestors in all.
7 later devices descend from it; 4 cite it directly.
0 of 10 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K083876: Sfi-Bar System Complete 2-Implant and 4-Implant, Cendres & Metaux SA (2010) Summary page 1.
- K102382: Sfi-Bar Implant Adapter Straumann, Sfi-Bar Implant Adapter for Neoss Implant, Cendres & Metaux SA (2010) Summary page 1.

## Most influential descendants
- K132814: Sfi-Bar Implant Abutments (2014), 6 descendants of its own
- K143051: ArgenIS Titanium Abutments (2015), 2 descendants of its own
- K160248: ArgenIS Titanium Abutments (2016), 1 descendant of its own
- K142407: Straight Stud Attachment (2014), 1 descendant of its own
- K172430: ArgenIS Titanium Abutments (2018), 0 descendants of its own

## Indications for use
The SF1-Bar® Implant Abutments are indicated to be used with dental implants as a prosthetic framework to support and /or retain removable or fixed dental prostheses in the treatment of partially or totally edentulous patients to restore chewing function. The abutment screws are intended to secure the bar to the endosseous implants.

Source page: https://510kreport.com/device/K130183
Methodology: https://510kreport.com/methodology