# K171068: OrthoView 7.2

- Pathway: 510(k) (Traditional)
- Applicant: Meridian Technique, Ltd.
- Decided: Oct 18, 2017 after 191 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: 8 generations back to K896095 (1990). 11 ancestors in all.
No later device cites it as a predicate yet.
0 of 12 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K063327: Orthoview, Merdian Technique, Ltd. (2006) Summary page 5.

## Indications for use
OrthoView is indicated for use when a suitable licensed and qualified healthcare professional requires access to medical images with the intention of using such images to plan or review a surgical procedure. OrthoView provides a set of tools and templates (representing prosthetic and fixation devices) to assist the healthcare professional in planning their surgery. The device is not to be used for mammography.

Source page: https://510kreport.com/device/K171068
Methodology: https://510kreport.com/methodology