# K141120: Zimmer ZFX Titanium Abutment for Straumann Bone Level Implant System

- Pathway: 510(k) (Traditional)
- Applicant: Zimmer Dental, Inc.
- Decided: Jul 29, 2014 after 90 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: 10 generations back to K894595 (1990). 85 ancestors in all.
No later device cites it as a predicate yet.
0 of 86 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K120873: Zimmer ZFX Abutment for Nobel Replace Implant System, Zimmer Dental, Inc. (2012) Summary page 1.
- K072151: P.004 RC Cares Titanium and Ceramic Abutments, Straumann USA (2007) Summary page 1.
- K081005: P.004 NC Cares Titanium and Ceramic Abutments, Institut Straumann AG (2008) Summary page 1.
- K071357: P.004 NC Anatomic Abutments, Institut Straumann AG (2007) Summary page 1.

## Indications for use
The Zimmer Zfx Titanium Abutment for Straumann Bone Level Implant System is designed for use as a terminal or intermediate abutment for cement retained prostheses. The abutment can be used with Straumann Bane Level implants with a Narrow CrassFht Connection (NC) 03.3mm or Regular Crossflt Connection (RC) 04.1 mm or 04.8mm.

Source page: https://510kreport.com/device/K141120
Methodology: https://510kreport.com/methodology