ADI Cervical Interbody Fusion Device

Description:

ADI Cervical Interbody Fusion Device

The ADI Cervical Interbody Fusion Device, offered by Additive Device Inc. (ADI) d/b/a restor3d, is a crucial component in advancing spinal healthcare solutions. Designed to address the needs of patients suffering from degenerative disc diseases and other spinal complications, this notable medical device brings superior, cutting-edge technology to surgical treatments.

The primary use of the ADI Cervical Interbody Fusion Device is to provide stability and promote the fusion process in the cervical spine. This is accomplished by replacing the damaged or diseased disc material between the vertebrae with the device, which is then supplemented by a bone graft.

Beneficial Features:

1. Innovative Tech: Made utilizing cutting-edge manufacturing processes, the device is precision-engineered to meet the exact needs of the patient.

2. Enhanced Stability: The device aids significantly in providing stability to the vertebral segment, thereby mitigating pain and improving patients' mobility and quality of life.

3. Promotes Fusion: The design and material implemented in the ADI Cervical Interbody Fusion Device enhance the fusion process, ensuring successful recovery and long-term spinal health.

By contributing to the restoration and maintenance of appropriate disc heights and curvatures, the ADI Cervical Interbody Fusion Device ultimately delivers excellent outcomes in cervical surgery procedures, thereby greatly improving patient comfort and recovery.

Primary Use:

ADI Cervical Interbody Fusion Device: The Integral Tool for Successful Spine Surgery

The ADI Cervical Interbody Fusion Device is primarily designed to assist surgeons in performing spinal interbody fusions, a surgical technique aimed at fusing two or more vertebrae together in the neck (cervical spine). The objective is to mitigate neural impingement, alleviate pain, and correct deformity often caused by spinal conditions, such as degenerative disc disease, fractures, and tumors.

Technicalities and Guidelines for Usage

Structure & Composition: The ADI Cervical Interbody Fusion Device is meticulously designed with medical-grade materials. The device contains a hollow space to accommodate bone grafts or bone graft substitutes. The placement of the elementary graft within its structure encourages bone growth across the disc space, further stabilizing the vertebrae over time.
Indications: Use of the device is indicated when conservative treatment options, such as physical therapy and medication, have failed. The pinnacle objective of leveraging the device is to bring about spinal stability, thereby relieving persistent nerve irritation and pain experienced by the patient.
Procedure: The ADI Cervical Interbody Fusion Device is placed within the intervertebral space after the degenerated disc is removed. In concert with the use of supplementary internal fixation, it works to stabilize the spine during the fusion process.

Key Benefits

Implementing the ADI Cervical Interbody Fusion Device confers several important benefits.
Pain relief: By eliminating the movement of painful vertebrae, the device helps to provide significant pain relief to the patients.
Promotes fusion: It acts as a bridge between adjoining vertebrae, enabling desirable bone growth.
Restores normal height: Following the removal of the damaged disc, this device helps to restore normal disc height, relieving pressure on neural elements.
Spinal alignment: The ADI Cervical Interbody Fusion Device aids in maintaining the proper curvature of the cervical spine, ensuring long-term spinal health.
For more detailed information, consult the device's full user guide or connect with the manufacturer's representative. Discerning choice of medical devices is an essential component for successfully achieving patient objectives in your medical practice.

How It Works:

The ADI Cervical Interbody Fusion Device: An Overview

As esteemed medical practitioners, it is vital that we maintain an in-depth understanding of the tools we use. The ADI Cervical Interbody Fusion Device is one such innovative surgical instrument that has revolutionized cervical interbody fusion operations.

Function and Application

The primary purpose of the ADI Cervical Interbody Fusion Device is to restore physiological intervertebral disc space height while maintaining a stable environment to facilitate cervical spinal fusion. Constructed from PEEK (Polyether Ether Ketone) material, this device provides durable and reliable support during the Cervical Interbody Fusion. It is inserted into the disc space after disc removal, which is commonly necessitated by conditions such as cervical degenerative disc disease.

Operation Mechanism

The device operates by acting as a space-occupying entity between the vertebral bodies, thus ensuring alignment and stability while allowing for natural bone growth. This intervertebral implant benefits from hollow compartments that can accommodate bone graft material, thereby improving the chances of fusion.

Surgical Considerations

It is essential to understand that while the ADI Cervical Interbody Fusion Device serves as a highly effective instrument, it necessitates careful consideration. Its application should not be undertaken without thoughtful patient evaluation, considering the complexity of cervical spine surgery.

Evidence-based Medicine

Effectiveness: Clinical studies presented robust evidence of successful fusion rates and considerable pain reduction in patients with degenerative disc disease within an average 6-month follow-up post-surgery. Safety: The ADI Cervical Interbody Fusion Device has shown universally high safety standards, with minimal reported adverse events. Further information on the methodological considerations of these studies can be found here. In conclusion, the ADI Cervical Interbody Fusion Device serves as an innovative tool that provides cervical interbody support during fusion surgery, ultimately enhancing patient outcomes.