Interspinous Implant Removable End Portion

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Solution Overview

Problem

Current interspinous process implants for treating spinal stenosis are invasive and do not allow for reduction in size after implantation, which can lead to prolonged recovery and discomfort for patients.

Innovation Solution

An interspinous process implant system with a detachable proximal end portion that can be removed post-implantation, utilizing various connection methods such as threaded, frangible, interference fit, or interlocking structures, allowing for reduction in size and profile after installation.

Engineering Contradictions & Design Principles

VSEngineering Contradiction Analysis

1Reliability

If a permanent interspinous process implant is used, then the implant provides continuous support and stability, but the implant maintains a large size and profile that can cause prolonged discomfort

Engineering Contradiction:
Improvecontinuous support and stabilityVSAvoidimplant size and profile
Core Design Contradiction:
ReliabilityVSLength of stationary object

Solution Approach 1:

The implant body is divided into two separate portions: a main body portion that remains in the interspinous space to provide continuous support, and a removable body portion that can be detached after implantation to reduce the overall size and profile of the device

Inventive Principle:
Principle #1Segmentation

Solution Approach 2:

The removable body portion is designed to be discarded after serving its temporary purpose during the initial healing phase, allowing the patient to experience reduced discomfort and improved mobility while the main body portion continues to provide stabilization

Inventive Principle:
Principle #34Discarding and recovering

2Length of stationary object

If a removable body portion is added to the implant, then the implant size can be reduced after implantation, but the device complexity increases

Engineering Contradiction:
Improveimplant size reductionVSAvoidtwo-part implant structure
Core Design Contradiction:
Length of stationary objectVSDevice complexity

Solution Approach 1:

The implant body is segmented into a main body portion and a removable body portion connected by a separable connection, allowing size reduction while maintaining relatively simple individual components that can be manufactured and assembled straightforwardly

Inventive Principle:
Principle #1Segmentation

3Loss of substance

If biodegradable materials are used for the removable body portion, then the implant can be fully absorbed by the body over time, but the manufacturing precision requirements increase

Engineering Contradiction:
Improvebiodegradation and absorptionVSAvoidmaterial composition control
Core Design Contradiction:
Loss of substanceVSManufacturing precision

Solution Approach 1:

The removable body portion is made from biodegradable material with controlled composition and degradation rate parameters, allowing it to maintain structural integrity during the initial healing period while gradually being absorbed by the body over time

Inventive Principle:
Principle #35Parameter changes

Solution Approach 2:

By separating the implant into biodegradable removable portion and non-biodegradable main body portion, the manufacturing precision requirements are distributed across different materials with appropriate properties for each function

Inventive Principle:
Principle #1Segmentation

Data Source

PatentEP3297554B1Interspinous process implant having a body with a removable end portion
Publication Date: 2024.04.24 SPINAL SIMPLICITY LLC
  • EP3297554B1 patent drawingFigure 1~2
  • EP3297554B1 patent drawingFigure 3
  • EP3297554B1 patent drawingFigure 4

AI summary

An interspinous process implant is disclosed that includes an elongated threaded implant body defining a longitudinal axis and having a main body portion with opposed proximal and distal end portions, and a removable body portion operatively connected to the proximal end portion of the main body portion, a distal anchor assembly including two deployable anchor blades mounted for pivotal movement between a stowed position located within an interior cavity of the main body portion and a deployed position radially extending from the main body portion, and a proximal anchor assembly including an anchor collar mounted for longitudinal movement along the longitudinal axis of the implant body between a first position spaced apart from the distal anchor assembly and a second position approximated with the distal anchor assembly.