# K173247: Surgical Planning Software version 1.1

- Pathway: 510(k) (Special)
- Applicant: Ortho Kinematics, Inc.
- Decided: Nov 8, 2017 after 33 days
- Product code: LLZ (System, Image Processing, Radiological)
- Device class: 2
- Regulation: 21 CFR 892.2050
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 11 generations back to K896095 (1990). 24 ancestors in all.
No later device cites it as a predicate yet.
0 of 25 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K171617: OKI Surgical Planning Software, Ortho Kinematics, Inc. (2017) Summary page 4.

## Indications for use
The Surgical Planning Software assists healthcare professionals in planning lumbar spinal fusion surgeries. The device allows service providers to plan surgical procedures, including tools for assessing anatomical components for placement of surgical implants. Clinical judgment and experience are required to properly use the software.

Source page: https://510kreport.com/device/K173247
Methodology: https://510kreport.com/methodology