# K072624: Astra Tech Implant System, New Component

- Pathway: 510(k) (Special)
- Applicant: Astra Tech AB
- Decided: Oct 1, 2007 after 14 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.
301 later devices descend from it; 5 cite it directly.
0 of 302 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) Astra Tech Implant System: named in the summary without a submission number

## Most influential descendants
- K120414: Osseospeed Plus (2012), 196 descendants of its own
- K081786: Ziocera & Convertible System (2008), 123 descendants of its own
- K100245: HS/HG Prosthetic System (2010), 111 descendants of its own
- K110308: Prosthetic System (2011), 105 descendants of its own
- K170588: DESS Dental Smart Solutions (2017), 86 descendants of its own

## Indications for use
Astra Tech Implant System abutments are intended to be used in conjunction with Astra Tech Implant System implants in fully edentulous or partially edentulous maxillary and/or mandibular arches to provide support for crowns, bridges or overdentures.

Source page: https://510kreport.com/device/K072624
Methodology: https://510kreport.com/methodology