# K961736: 17 Angulated Abutment

- Pathway: 510(k) (Traditional)
- Applicant: Nobelpharma USA, Inc.
- Decided: Jul 18, 1996 after 76 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
Longest line of descent: 1 generation back to K944962 (1995). 1 ancestor in all.
8 later devices descend from it; 1 cites it directly.
0 of 10 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K944962: Branemark System 17 Angulated Abutment, Nobelpharma USA, Inc. (1995) Summary page 1.

## Most influential descendants
- K200992: S.I.N. Dental Implant System (2020), 7 descendants of its own
- K211921: S.I.N. Dental Implant System (2021), 5 descendants of its own
- K222231: S.I.N. Dental Implant System (2022), 4 descendants of its own
- K221453: S.I.N. Dental Implant System (2022), 1 descendant of its own
- K252266: S.I.N. Dental Implant System (2025), 0 descendants of its own

## Indications for use
Intended to be used in edentulous patients as an anchor to support a prosthesis.

Source page: https://510kreport.com/device/K961736
Methodology: https://510kreport.com/methodology