# K080450: Stryker Power Tool Navigator Attachment

- Pathway: 510(k) (Traditional)
- Applicant: Stryker Corp.
- Decided: Jul 17, 2008 after 149 days
- Product code: HAW (Neurological Stereotaxic Instrument)
- Device class: 2
- Regulation: 21 CFR 882.4560
- 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 K993239 (2000). 3 ancestors in all.
1 later device descends from it; 1 cites it directly.
0 of 5 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K993239: Stryker Navigation System - Neuro Module, Model 6000-XXX-XXX, Stryker Corp. (2000) Summary page 1.
- K010204: Stryker Navigation System-Knee Module, Stryker Corp. (2001) Summary page 1.
- K022365: Stryker Navigation System - Hip Module, Stryker Instruments (2003) Summary page 1.

## Most influential descendants
- K160523: BrightMatter Guide with BrightMatter Pointer (2016), 0 descendants of its own

## Indications for use
The Stryker® Power Tool Navigator attachment is intended to enable spatial localization and identification of Stryker Power Tools by the Stryker® Navigation System.

Source page: https://510kreport.com/device/K080450
Methodology: https://510kreport.com/methodology