# K073714: Traumacad Version 2.0

- Pathway: 510(k) (Traditional)
- Applicant: Orthocrat, Ltd.
- Decided: Mar 19, 2008 after 79 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: 7 generations back to K896095 (1990). 20 ancestors in all.
117 later devices descend from it; 13 cite it directly.
0 of 138 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K042816: Traumacad 1.2, Orthocrat, Ltd. (2004) Summary page 1.
- K071972: Orthopedic Software for Impax Workstations, Agfa Healthcare Corp. (2007) Summary page 1.

## Most influential descendants
- K111019: Surgimap (TM) Spine (2011), 51 descendants of its own
- K142923: TraumaCad Mobile Release 1.0 (2015), 28 descendants of its own
- K141669: Surgimap (2014), 27 descendants of its own
- K160284: JointPoint (2016), 21 descendants of its own
- K163221: Mazor X (2017), 19 descendants of its own

## Indications for use
The TraumaCAD program is indicated for assisting healthcare professionals in preoperative planning of orthopedic surgery. The device allows for overlaying of prosthesis templates on radiological images, and includes tools for performing measurements on the image and for positioning the template. Clinical judgments and experience are required to properly use the software.

Source page: https://510kreport.com/device/K073714
Methodology: https://510kreport.com/methodology