# K000310: Voyager 6.0 Software Option

- Pathway: 510(k) (Special)
- Applicant: Philips Medical Systems (Cleveland), Inc.
- Decided: Feb 15, 2000 after 14 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.
190 later devices descend from it; 3 cite it directly.
0 of 191 devices in its family (counting itself) have 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
- K023975: Voyager Linux (2002), 172 descendants of its own
- K013025: Modification to Flourolab Plus (2001), 151 descendants of its own
- K031454: Acumen Surgical Navigation System (2004), 146 descendants of its own
- K050973: Modification to: Voyager Linux (2005), 97 descendants of its own
- K052851: Voyager Linux with Tactile Guidance System (TGS) (2005), 96 descendants of its own

Source page: https://510kreport.com/device/K000310
Methodology: https://510kreport.com/methodology