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FRACTURES AND DEFORMITIES
MAXFRAME™ Software
FRACTURES AND DEFORMITIES
MAXFRAME™ Software
The MAXFRAME™ 3D/3D II Software is a treatment planning software and part of the MAXFRAME™ Multi-Axial Correction System. The MAXFRAME™ 3D Software/MAXFRAME™ 3D II Software provides a dynamic visualization of the patient treatment plan, letting the surgeon plan for success even before adjusting the first strut.1,◊ The software includes planning methods, treatment plan simulation, calculation and review of strut adjustment plans, review of strut swap dates, treatment plan sharing with other users, and patient and case management.
IMAGES
Key Resources
Software User Manuals
Instructions for Use
Surgeon Planning Worksheet
Learn More about the MAXFRAME™ 3D II Software
SOFTWARE ADVANCEMENTS
MAXFRAME™ 3D II Software – Now Available!
Introduced in 2021, the MAXFRAME™ 3D II Software is similar to the original software and offers usability and interface improvements with additional functionality.
The MAXFRAME™ 3D II Software provides surgeons with several updated features and functions including:
- Increased interface improvements, such as better use of the screen space and larger fonts
- The phases feature which allows surgeons to define up to 5 treatment plan phases, enabling increased surgeon control* over the deformity correction plan2,◊
- The ability for foot plates to be used proximally
- Improved strut rendering*
- The ability for struts to be flipped more accurately in the strut rendering area to better reflect the way the frame was installed on the patient
*compared to MAXFRAME™ 3D Software
DESIGNED TO INCREASE TREATMENT PLAN ACCURACY5
Perspective Frame Matching (PFM) Planning Method
The MAXFRAME™ Software with Perspective Frame Matching (PFM) Technology uses post operative x-rays to generate the deformity and mounting parameters for a strut adjustment plan and is designed to increase the treatment plan accuracy.5,◊
The software with PFM technology does not require x-ray scaling, or strict adherence to the use of orthogonal x-rays. This may increase the treatment plan accuracy and reduce procedure complexity as compared to systems which require data to be measured from patient x-rays and manually entered into the software.◊
- Less strict requirement for orthogonal mounting of the reference ring, as the software is designed to accommodate for ring tilt.3,4,◊
- Does not require x-ray scaling, or strict adherence to the use of orthogonal x-rays.3,4,◊
- Software calculates deformity and mounting parameters
- Requires only one post-operative A/P and Lateral X-ray to be uploaded
References
- DePuy Synthes Functional & Design Requirements and Verification & Validation Matrix. 13/04/2021. Windchill Document# 0000088795
- DePuy Synthes System Requirement Verification - Run1 . 23/03/2021. Subversion Document D3_09_61_520_System_requirements_verification_Run_1
- DePuy Synthes Software Test Report. 13/09/2016. Windchill Document #0000260164.
- DePuy Synthes Software Test Report. 13/09/2016. Windchill Document #0000260249.
- DePuy Synthes Software Test Report. 13/09/2016. Windchill Document #0000260163
◊Non-Clinical Evidence
Indications and Contraindications
Indications
The DePuy Synthes MAXFRAME™ System and MAXFRAME AUTOSTRUT™ System is indicated for the following treatments in adults, and in both children (3-12) and adolescents (12-21) in which growth plates have fused or will not be crossed with hardware: fracture fixation (open and closed), pseudoarthrosis of long bones, limb lengthening (epiphyseal or metaphyseal distraction), joint arthrodesis, infected fractures or non-unions, correction of bony or soft tissue deformities, correction of segmental defects.
Contraindications
MAXFRAME™ and MAXFRAME AUTOSTRUT™ is not intended for use in the spine.
Please refer to the instructions for use for a complete list of indications, contraindications, warnings and precautions.
225836-220902 DSUS
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