# K200350: MyHip Planner & Verifier

- Pathway: 510(k) (Traditional)
- Applicant: Medacta International S.A.
- Decided: Nov 4, 2020 after 266 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: 10 generations back to K896095 (1990). 26 ancestors in all.
1 later device descends from it; 1 cites it directly.
0 of 28 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K170702: mediCAD 4.0, Medicad Hectec GmbH (2018) Summary page 4.
- K160284: JointPoint, Jointpoint, Inc. (2016) Summary page 4.

## Most influential descendants
- K221725: Advanced MyHip Planner (2023), 0 descendants of its own

## Indications for use
The MyHip Planner software is intended for image processing and pre-operative planning of acetabular cup and femoral stem positioning for Total Hip Arthroplasty (THA). The device assists the user in assessing potential leg length and offset differences as well as potential range of motion impingement. The MyHip Verifier software is intended to assist in the intra-operative evaluation of leg length and offset differences as well as acetabular cup positioning for anterior approach Total Hip Arthroplasty when the patient is positioned supine.

Source page: https://510kreport.com/device/K200350
Methodology: https://510kreport.com/methodology