# K081851: Neoss Access Abutments

- Pathway: 510(k) (Traditional)
- Applicant: Neoss, Ltd.
- Decided: Mar 2, 2009 after 245 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: 8 generations back to K894595 (1990). 21 ancestors in all.
No later device cites it as a predicate yet.
0 of 22 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K061477: Multi-Unit Abutments for Astratech, Camlog and Ankylos Implant Systems, Nobel Biocare AB (2006) Summary page 1.

## Indications for use
The Neoss Access Abutments are designed to be connected to the Neoss implants and intended for use as an aid in prosthetic rehabilitation. Neoss Access Abutments represent a two piece abutment system and are designed to be connected to the Neoss implants, to receive another abutment or framework and intended for use as an aid in multiple-unit prosthetic rehabilitation such as dental bridge restorations.

Source page: https://510kreport.com/device/K081851
Methodology: https://510kreport.com/methodology