# K072899: Orthopilot 2 Total Hip Arthroplasty (Tha) Version 3.0

- Pathway: 510(k) (Special)
- Applicant: Aesculap Implant Systems, Inc.
- Decided: Feb 6, 2008 after 118 days
- Product code: HAW (Neurological Stereotaxic Instrument)
- Device class: 2
- Regulation: 21 CFR 882.4560
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 3 generations back to K003347 (2001). 6 ancestors in all.
No later device cites it as a predicate yet.
0 of 7 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K050752: Aesculap Orthopilot 2 Tha V 2.0, Aesculap, Inc. (2005) Summary page 2.
- K013569: Orthopilot 2, Aesculap, Inc. (2002)

## Indications for use
The Orthopilot® 2 Navigation Platform is a system for computer-aided navigation of surgical instruments. Its purpose is to optimally position endoprosthesis in arthroplasty such as the Search Evolution Knee system and the Gem Knee system in the patient. It aids the surgeon in accurately positioning the cutting guides, drills and reamers for total endoprosthesis replacement surgery and provides intraoperative measurements of bone alignment. It indicates optimized angles and positions for implant placement.

Source page: https://510kreport.com/device/K072899
Methodology: https://510kreport.com/methodology