# K132244: N-Force Fixation System

- Pathway: 510(k) (Traditional)
- Applicant: Innovision, Inc.
- Decided: Mar 6, 2014 after 231 days
- Product code: HWC (Screw, Fixation, Bone)
- Device class: 2
- Regulation: 21 CFR 888.3040
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 11 generations back to K960978 (1996). 78 ancestors in all.
3 later devices descend from it; 2 cite it directly.
0 of 82 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K102528: N-Force Fixation System, Innovision, Inc. (2011) Summary page 2.

## Most influential descendants
- K151146: N-Force Fixation System (2015), 1 descendant of its own
- K142776: Flow-Screw (2015), 1 descendant of its own
- K173556: Injection Screw (2018), 0 descendants of its own

## Indications for use
The N-Force Fixation System is intended for the fixation of bone fractures and bone reconstructions. When used for these indications, the N-Force Fixation System can also be used to deliver the following bone void fillers to a surgical site: * Beta-bsm (ETEX Corporation) * Carrioen (ETEX Corporation)

Source page: https://510kreport.com/device/K132244
Methodology: https://510kreport.com/methodology