# K151490: Prettau Anterior T0

- Pathway: 510(k) (Traditional)
- Applicant: Zirkonzahn GmbH
- Decided: Oct 8, 2015 after 127 days
- Product code: EIH (Powder, Porcelain)
- Device class: 2
- Regulation: 21 CFR 872.6660
- 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 K061851 (2006). 2 ancestors in all.
No later device cites it as a predicate yet.
0 of 3 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K132230: Ice Zirkon Transluzent, Zirkonzahn Srl (2014) Summary page 4.

## Indications for use
PRETTAU® ANTERIOR TO is intended to be used for the manufacturing of metal free single-unit anterior and posterior prostheses, inlays, onlays, veneers bonded dental restorations.

Source page: https://510kreport.com/device/K151490
Methodology: https://510kreport.com/methodology