Transsacral Spinal Implant Segmentation and Composite Design

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Solution Overview

Problem

Current spinal stabilization and arthrodesis techniques, particularly in minimally invasive spinal surgery, face limitations in achieving flexible and stable spinal fusion while minimizing trauma and adverse events, such as loss of spinal alignment and subsidence, especially in complex spinal disorders with varying anatomical conditions.

Innovation Solution

The development of preformed cages, spacers, and plugs made from biocompatible materials like titanium, Nitinol, and PEEK, which can be implanted via a trans-sacral approach to provide additional stability, flexibility, and strength, allowing for axial and lateral deployment within the disc space, and are designed to promote bone growth and prevent subsidence.

Engineering Contradictions & Design Principles

VSEngineering Contradiction Analysis

1Reliability

If traditional spinal stabilization techniques are used, then spinal fusion can be achieved, but trauma to surrounding tissues and loss of spinal alignment occur

Engineering Contradiction:
Improvespinal fusion successVSAvoidtissue trauma and alignment loss
Core Design Contradiction:
ReliabilityVSObject-affected harmful factors

Solution Approach 1:

The implant is divided into multiple functional segments: a sacral portion for anchoring in the sacrum, a body portion for receiving bone graft, and an interbody portion for spinal fusion. This segmentation allows each portion to be optimized for its specific function while minimizing overall trauma through the transsacral approach

Inventive Principle:
Principle #1Segmentation

Solution Approach 2:

The implant serves as an intermediary device between the sacrum and the spinal vertebrae, providing a stable bridge that maintains alignment while allowing minimally invasive insertion. The device mediates the load transfer and structural support without requiring extensive dissection of surrounding tissues

Inventive Principle:
Principle #24Intermediary (Mediator)

2Object-affected harmful factors

If minimally invasive trans-sacral approach is used, then tissue trauma is reduced, but implant stability and strength are compromised

Engineering Contradiction:
Improvetissue traumaVSAvoidimplant stability
Core Design Contradiction:
Object-affected harmful factorsVSStrength

Solution Approach 1:

The implant utilizes composite material properties combining a rigid sacral portion for secure anchoring with a porous body portion for bone ingrowth. This composite structure achieves both minimal insertion trauma and maximum long-term stability through biological integration

Inventive Principle:
Principle #40Composite materials

Solution Approach 2:

The body portion of the implant features a porous structure that allows bone tissue to grow into and through the device. This porous architecture provides mechanical interlocking strength while maintaining the minimally invasive nature of the transsacral insertion approach

Inventive Principle:
Principle #31Porous materials

3Adaptability or versatility

If flexible implant design is used, then adaptation to varying anatomical conditions is improved, but structural strength and stability are reduced

Engineering Contradiction:
Improveanatomical adaptationVSAvoidstructural stability
Core Design Contradiction:
Adaptability or versatilityVSStrength

Solution Approach 1:

The implant incorporates dynamic elements including a resilient interbody portion that can flex and adapt to the natural movement and varying anatomy of the spinal column. This dynamic design maintains structural integrity while accommodating physiological motion and anatomical variations

Inventive Principle:
Principle #15Dynamics

Data Source

PatentUS9814598B2Spinal implants and implantation system
Publication Date: 2017.11.14 MIS IP HOLDINGS LLC
  • US9814598B2 patent drawing
  • US9814598B2 patent drawing
  • US9814598B2 patent drawing

AI summary

Disclosed are surgical implants for providing therapy to a treatment site, tool sets and methods for percutaneously accessing and deploying the implants within the spines. The treatment site may be a vertebral body, disc, and/or motion segments in the lumbar and sacral regions of the spine.