# K941393: Iti Angled Abutment

- Pathway: 510(k) (Traditional)
- Applicant: The Straumann Co.
- Decided: Jun 14, 1995 after 449 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.
177 later devices descend from it; 1 cites it directly.
0 of 178 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA has not posted a summary or statement for it, so its predicates are not known.

## Most influential descendants
- K962647: Angled Abutment (1996), 176 descendants of its own
- K994119: Synocta Angled Abutments (2000), 175 descendants of its own
- K080239: P.004 Abutments,  P.004 Temporary Copings, P.004 Protective Caps, P.004 Permanent Copings (2008), 164 descendants of its own
- K133421: Straumann Magellan (TM) Abutment,Protective Cap,Titanium Copings,Gold Chopings,Basal Screw (2014), 115 descendants of its own
- K150367: Neodent Implant System (2015), 89 descendants of its own

Source page: https://510kreport.com/device/K941393
Methodology: https://510kreport.com/methodology