# K946033: Leibinger Stereoplan Plus Sterotactic Treatment Plan Ing Software Package

- Pathway: 510(k) (Traditional)
- Applicant: Leibinger GmbH
- Decided: Sep 1, 1995 after 266 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 K892425 (1990). 1 ancestor in all.
1 later device descends from it; 1 cites it directly.
0 of 3 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K892425: STP Complete Module Set, Leibinger & Fischer, Ltd. (1990) Summary page 2.

## Most influential descendants
- K110644: Praezis Plus (2012), 0 descendants of its own

## Indications for use
The Stereoplan Plus system is intended to be used in planning stereotactic treatment of intracerebral lesions. Specifically, the Stereoplan Plus system is intended for planning stereotactic punctures.

Source page: https://510kreport.com/device/K946033
Methodology: https://510kreport.com/methodology