IntelliGuide®
Patient-Specific 3D Bunion Correction
The first patented patient-specific cut guides for personalized 3D bunion and midfoot correction in the US.
IntelliGuide® Provides
- Intelligent pre-op planning.
Simplifies complexity by visualizing and determining your triplanar correction before entering the OR. - Patient-specific 3D correction.
3D printed titanium cut guides with customized correction designed to match each patient’s unique anatomy. - Streamlined surgical workflow.
Drive OR efficiency with fewer steps and less instrumentation regardless of the level of severity.1
IntelliGuide® Customer Process
Step 1: Submit Files
Medical images are uploaded per protocol
Step 2: Pre-Op Plan
The deformity is corrected based on pre-op parameters and surgeon approval
Step 3: Personalized Surgery2
Patient-Specific guides with models are sent for surgery
IntelliGuide® for Lapiplasty®
Step 1: Cut
Step 2: Compress
Step 3: Fixate*
IntelliGuide® for Adductoplasty®
Step 1: Cut
Step 2: Compress
Step 3: Fixate*
Supporting Documents
CT Scan and WB X-Ray Protocol
Surgical Technique Using Lapiplasty® PSI Cut Guide
Surgical Technique Using Adductoplasty® PSI Cut Guide
Instructions for Use
Other Products
Lapiplasty®
The first and only comprehensive system
designed for reproducible realignment, stabilization, and fusion of the midfoot in the US.
Adductoplasty®
Relentless innovation drives best-in-class outcomes and OR efficiency.
Biologics & Wedges
Treace™ Allograft Wedges are engineered for strength and correction. CortiFuse™ maximizes healing potential with every fiber.
Got Questions?
For more information or to get trained on Treace’s comprehensive 3D Bunion Correction® systems, give us a call or complete the form.
*Construct is at the surgeon’s discretion and shown for illustrative purposes only. Proceed with the preferred fixation system per the respective surgical technique.
**Dr. Mark Easley is a paid consultant for Treace Medical Concepts.
BoneClone™ models are gray
1. TMC data on file across multiple instrumented Lapidus procedures.
2. TMC PSI products are not a “custom device” per Sec 520(b) of the FD&C Act; they are patient-specific, fit to the patient with their own CT scans per 21 CFR Part 888.3030.
M3931B