# K160581: K3PRO Konus Additional Abutments and Implants

- Pathway: 510(k) (Traditional)
- Applicant: Argon Med. Productions Vertriebs Gesellschaft Mbh CO KG
- Decided: Mar 24, 2017 after 388 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.
1 later device descends from it; 1 cites it directly.
0 of 2 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. The FDA summary names no predicate by number.

## Most influential descendants
- K190192: K3Pro Konus New Abutments and Implants (2020), 0 descendants of its own

## Indications for use
K3Pro Konus Additional Abutments and Implants are designed to be compatible with the K3Pro Konus Dental Implant system and are for use in edentulous sites in the mandible or maxilla for support of a complete denture prosthesis, a final or intermediate abutment for fixed bridgework or for partial dentures, or as a single tooth replacement. Delayed loading is recommended. The prosthesis may be secured to the abutment by the use of adhesives or mechanically by the use of a screw.

Source page: https://510kreport.com/device/K160581
Methodology: https://510kreport.com/methodology