# K211876: Intellijoint VIEW

- Pathway: 510(k) (Traditional)
- Applicant: Intellijoint Surgical, Inc.
- Decided: Nov 12, 2021 after 148 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). 26 ancestors in all.
No later device cites it as a predicate yet.
0 of 27 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 4.
- K203651: Cuptimize, Cuptimize, Inc. (2021) Summary page 4.

## Indications for use
Intellijoint VIEW is indicated to assist qualified healthcare professionals in preoperative planning and postoperative review of orthopedic surgery. The device allows for orthopedic implant templates to be overlaid on medical images for the purpose of selecting and positioning implants. The device includes tools for performing measurements and evaluating surgical treatment options. Clinical judgement and experience are required to properly use the software.

Source page: https://510kreport.com/device/K211876
Methodology: https://510kreport.com/methodology