# K242272: CORIOGRAPH Pre-Op Planning and Modeling Services

- Pathway: 510(k) (Traditional)
- Applicant: Blue Belt Technologies, Inc.
- Decided: Nov 15, 2024 after 106 days
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 23 generations back to K905070 (1991). 126 ancestors in all.
1 later device descends from it; 1 cites it directly.
0 of 128 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K240113: CORIOGRAPH Knee Pre-Op Plan, Smith & Nephew, Inc. (2024) Summary page 5.
- K212040: RI.Hip Modeler, Blue Belt Technologies, Inc. (2022) Summary page 5.

## Most influential descendants
- K250921: CORIOGRAPH Pre-Op Planning and Modeling Services (2025), 0 descendants of its own

## Indications for use
Intended Use CORIOGRAPH Pre-Op Planning and Modeling Services are intended to provide preoperative planning for surgical procedures based on patient imaging, provided that anatomic landmarks necessary for generating the plan are identifiable on patient imaging scans. Indications for Use The CORIOGRAPH Pre-op Planning and Modeling Services are indicated for use for the following procedures: • Unicondylar Knee Replacement (UKR) • Total Knee Arthroplasty (TKA) • Primary Total Hip Arthroplasty (THA)

Source page: https://510kreport.com/device/K242272
Methodology: https://510kreport.com/methodology