# K944962: Branemark System 17 Angulated Abutment

- Pathway: 510(k) (Traditional)
- Applicant: Nobelpharma USA, Inc.
- Decided: Feb 27, 1995 after 143 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.
32 later devices descend from it; 3 cite it directly.
0 of 33 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
- K052885: Zygoma 17 Abutment Multi-Unit RP 2MM, Model 29314; Zygoma 17 Abutment Multi-Unit RP 3MM, Model 29315 (2005), 20 descendants of its own
- K070182: Zygoma Implant (Immediate Function) (2007), 19 descendants of its own
- K093562: Endosseous Dental Implant (2010), 10 descendants of its own
- K141777: Neodent Implant System (2015), 8 descendants of its own
- K961736: 17 Angulated Abutment (1996), 8 descendants of its own

Source page: https://510kreport.com/device/K944962
Methodology: https://510kreport.com/methodology