# K072271: Stryker Navigation System Infinitus Hip Resurfacing Module

- Pathway: 510(k) (Traditional)
- Applicant: Stryker Corp.
- Decided: Dec 18, 2007 after 125 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: 4 generations back to K010612 (2001). 7 ancestors in all.
No later device cites it as a predicate yet.
0 of 8 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K022365: Stryker Navigation System - Hip Module, Stryker Instruments (2003) Summary page 1.
- K063028: Vectorvision Hip SR, Brainlab AG (2006) Summary page 1.

## Indications for use
The system is indicated for partial hip resurfacing, to assist in precise positioning of the femoral resurfacing component. The system should be operated only by trained personnel such as orthopedic surgeons and clinic staff.

Source page: https://510kreport.com/device/K072271
Methodology: https://510kreport.com/methodology