# K072100: GC Aadva Abutment

- Pathway: 510(k) (Abbreviated)
- Applicant: GC America, Inc.
- Decided: Feb 14, 2008 after 198 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.
3 later devices descend from it; 2 cite it directly.
0 of 4 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA lists a 510(k) statement for it but has not posted the file, so its predicates are not known.

## Most influential descendants
- K103234: GC Aadva BO AC Abutments (2011), 1 descendant of its own
- K141970: Digitek Titanium Abutment (2015), 0 descendants of its own
- K113816: GC Aadva Abutment- Zirconium-BO AC BH SV (2013), 0 descendants of its own

Source page: https://510kreport.com/device/K072100
Methodology: https://510kreport.com/methodology