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Intended for Healthcare Professionals

InCore®ÌýLapidus System

Three-part construct intended for internal fixation for First Tarsometatarsal Fusion.Ìý

InCore®ÌýLapidus System Precision Guided Correction
OverviewKey Data PointsSystem FeaturesSpecificationsBenefitsEducationVideosAdditional InformationRelated Products

Inspired. Intuitive. InCore.

This system is internal to the bone,Ìýand is designed to help minimizeÌýthe need for hardware removal due to pain and irritation reported with traditional external platingÌýconstructsÌýof first tarsometatarsal arthrodesis.1

Anatomy

  • Forefoot
  • Midfoot

Procedure

  • Forefoot: Lapidus
  • Midfoot: Lapidus

InCore® Lapidus is designed as a post and screws construct to minimize hardware prominence that can cause pain and lead to hardware removal

Hardware removal due to pain and irritation is reported in up to

17%

of first tarsometatarsal arthrodesis cases when using plating constructs.1,2

System Features

The kit contains the post and instruments needed for one procedure*,Ìýdesigned to eliminateÌýproductÌýcomplexity for hospital staff andÌýimproveÌýoperating room productivity.Ìý

System Features

Targeting Guide

  • Stabilizes correction in all three planes (transverse, sagittal, and frontal planes)

  • Provides distraction of joint for visualization and joint preparation

  • Intended to aid and hold pre-compression of joint

  • Designed to simplifyÌýthe technique with fully-guided steps

Disposable Option

  • Fully sterile implant and instrument system

  • Instrumentation has never been used, damaged, or worn prior to surgery

  • Time and cost savings of sterilization prior to case

  • The system is designed to beÌýeasy to useÌýand mitigateÌýcomplexity for surgical team, potentially increasing OR efficiency.

Specifications

Benefits

Fully Guided

  • Designed to simplifyÌýthe technique with fully-guided stabilize angular/rotational correction in all three planes. Distraction allows for properÌýjoint visualization and preparation allowing surgeon to cut, curettage or micro fracture. Additionally, the system has a built-in compression/distraction fixture intended to aid and hold pre-compression of the joint.

Solid IntermedullaryÌýConstruct

  • The system includes post and screws designed to minimize hardware prominence that can result in hardware removal due to pain or irritation related to such hardware prominence.Ìý Studies have shown up to 17% hardware removal due to pain and irritation when using plating constructs for first tarsometatarsal arthrodesis cases.1,2

Efficient

  • The easy to use, pre-sterilized kit was intended to decrease time, sterilization cost and contamination concerns. Instruments are new and sharp every timeÌýminimizingÌýthe complexity for the OR team. Intermedullary implant post comes pre-assembled to the compression/distraction guide, eliminating need for back table assembly.

Education

Literature

InCore Lapidus SystemÌýSurgical Technique

Surgical Approach The InCore® Lapidus System is designed to minimize the need for hardware removal due to pain and irritation reported with traditional external plating constructs of first tarsometatarsal arthrodesis.

Product Brochure

Inspired. Intuitive. InCore.

FEA Report

Strength Profile

Outcome Study

White Paper

An Intramedullary Fixation Device for the Modified Lapidus ProcedureÌý

Videos

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InCore Lapidus System Video

Watch video

Click to play video
InCore Lapidus System Animation

Watch animation

Click to play video
InCore Lapidus System Surgical Demonstration

Watch demonstration

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InCore Lapidus System Precision Guided Correction

Watch video

Additional Information

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This material is intended for health care 91³Ô¹ÏÍø. Distribution to any other recipient is prohibited.Ìý

For product information, including indications, contraindications, warnings, precautions, potential adverse effects and patient counseling information, see theÌýinstructions for use or contact your local representative; search this website for additional product information.ÌýTo obtain a copy of the current Instructions for Use (IFU) for full prescribing and risk information, please visit or callÌý1-800-348-2759, press 4 for 411 Technical Support.