# K073141: Spi Art Abutment

- Pathway: 510(k) (Special)
- Applicant: Thommen Medical AG
- Decided: Dec 5, 2007 after 28 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
No predicates in its family tree.
182 later devices descend from it; 1 cites it directly.
0 of 183 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 its predicate without a number.
- (no number) SPI ART Abutment: named in the summary without a submission number

## Most influential descendants
- K101207: Neodent Implant System (2010), 181 descendants of its own
- K101945: Neodent Implant System (2011), 180 descendants of its own
- K123022: Neodent Implant System (2013), 127 descendants of its own
- K133510: Neodent Implant System (2014), 123 descendants of its own
- K133421: Straumann Magellan (TM) Abutment,Protective Cap,Titanium Copings,Gold Chopings,Basal Screw (2014), 115 descendants of its own

## Indications for use
SPI® ART Abutment is intended to be used in conjunction with SPI® System dental implants in the maxillary and/or mandibular arch to provide support for crowns, bridges or overdentures. SPI ART Abutment is contraindicated for free-end bridges or bridges with more than one intermediate pontic element.

Source page: https://510kreport.com/device/K073141
Methodology: https://510kreport.com/methodology