# K002732: Stryker  Navigation System - Ent Module

- Pathway: 510(k) (Traditional)
- Applicant: Stryker Corp.
- Decided: Oct 2, 2000 after 31 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
No predicates in its family tree.
53 later devices descend from it; 3 cite it directly.
1 of 54 devices in its family (counting itself) has 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
- K062640: Stryker Navigation System - Cranial Module, Model 6000-650-000 (2006), 50 descendants of its own
- K131214: Cranial Map Neuro (2013), 26 descendants of its own
- K141941: Spinemask Tracker, Spinemap 3D 3.0-Software,Spinemap 3D 3.0-Upgreade, Spinemap  3D 3.0-Enable, Spinemap  3D 3.0-Sales D (2014), 22 descendants of its own
- K130874: Stryker NAV3I Platform (2013), 22 descendants of its own
- K141551: Profess Software, Profess Curved 70 (Degrees) Suction, Profess Curved 70 (Degrees) Suction, Profess Curved 90 (Degrees) (2014), 20 descendants of its own

Source page: https://510kreport.com/device/K002732
Methodology: https://510kreport.com/methodology