# K960714: Isg Viewing Wand

- Pathway: 510(k) (Traditional)
- Applicant: I.S.G. Technologies, Inc.
- Decided: May 29, 1996 after 98 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 K911783 (1994). 3 ancestors in all.
71 later devices descend from it; 3 cite it directly.
0 of 75 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K911783: Allegro Viewing Wand, I.S.G. Technologies, Inc. (1994) Summary page 2.
- K951262: Operating Arm System (Oas), Radionics Software Applications, Inc. (1995) Summary page 2.
- K944612: Acustar I Advanced Surgical Navigation System, Codman & Shurtleff, Inc. (1995) Summary page 2.
- (no number) Zeiss: named in the summary without a submission number

## Most influential descendants
- K964229: Regulus Navigator (1997), 66 descendants of its own
- K981315: Navitrack (1998), 36 descendants of its own
- K033413: Spineassist Device (2004), 35 descendants of its own
- K051676: Spineassist Device with Additional Accessories (2005), 34 descendants of its own
- K063607: Spineassist System (2007), 33 descendants of its own

Source page: https://510kreport.com/device/K960714
Methodology: https://510kreport.com/methodology