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PEEK Interbody Fusion Cage
The system consists of cervical and lumbar interbody fusion cages. The fusion cages are made from PEEK material (VESTAKEEP®i4R) compliant with YY/T 0660, while the radiopaque markers are made from pure tantalum compliant with YY/T 0966. The products are available in both non-sterile and sterile packaging, with the sterile versions being radiation-sterilized and having a shelf life of 5 years.
Product English Name:
PEEK Interbody Fusion Cage
Alias:
PEEK Cage,Spinal Fusion Device
Intended Use:
Designed to be used in conjunction with spinal fixation products, the PEEK Interbody Fusion Cage is intended for cervical and lumbar interbody fusion procedures. It aids in stabilizing the spine and promoting bone growth between vertebrae.
Product Introduction

The PEEK Interbody Fusion Cage is a state-of-the-art medical device designed to facilitate spinal fusion in both cervical and lumbar regions. Made from high-quality PEEK material, it offers excellent biocompatibility and mechanical strength, ensuring long-term stability and support. The inclusion of radiopaque markers made from pure tantalum allows for precise imaging during and after surgery.

1. The PEEK Interbody Fusion Cage is known for its exceptional biocompatibility and mechanical properties, making it an ideal choice for spinal fusion surgeries. Its design ensures minimal interference with imaging techniques, allowing for clear post-operative assessments.
2. Structurally, the cage is composed of PEEK material (VESTAKEEP®i4R), which is known for its durability and resistance to wear. The radiopaque markers are made from pure tantalum, providing excellent visibility under X-ray and other imaging modalities.
3. The primary use of the PEEK Interbody Fusion Cage is in spinal fusion surgeries, where it is used to stabilize the spine and promote bone growth between vertebrae. It is particularly effective in cervical and lumbar regions, offering a reliable solution for patients with degenerative disc disease or spinal instability.

The PEEK Interbody Fusion Cage, also known as the PEEK Cage or Spinal Fusion Device, is a highly reliable and effective solution for spinal fusion surgeries. Its unique composition and design make it a preferred choice among surgeons, offering both stability and clarity in post-operative imaging.

Main Features

The PEEK Interbody Fusion Cage offers a range of features designed to enhance spinal fusion outcomes, including excellent biocompatibility, mechanical strength, and radiopaque visibility.

1. The cage's PEEK material ensures high biocompatibility, reducing the risk of adverse reactions and promoting successful integration with the patient's bone structure.
2. Its mechanical strength provides long-term stability, crucial for the success of spinal fusion surgeries, especially in weight-bearing areas like the lumbar spine.
3. The inclusion of radiopaque markers made from pure tantalum allows for precise imaging, ensuring accurate placement and post-operative assessment.
4. The cage is available in both non-sterile and sterile versions, with the sterile option being radiation-sterilized and having a shelf life of 5 years, ensuring safety and reliability.
5. The design of the cage promotes bone growth between vertebrae, aiding in the fusion process and providing a stable environment for healing.

The PEEK Interbody Fusion Cage stands out for its combination of biocompatibility, mechanical strength, and imaging clarity. These features make it an indispensable tool in spinal fusion surgeries, offering both surgeons and patients a reliable and effective solution.

Clinical Applications

The PEEK Interbody Fusion Cage is widely used in clinical settings for spinal fusion surgeries, particularly in the cervical and lumbar regions, to treat conditions like degenerative disc disease and spinal instability.

1. In cervical spine surgeries, the cage is used to stabilize the vertebrae and promote fusion, often in cases of degenerative disc disease or trauma.
2. For lumbar spine surgeries, the cage provides essential support and stability, aiding in the fusion process and reducing pain associated with spinal instability.
3. The cage's radiopaque markers allow for precise placement during surgery, ensuring optimal outcomes and reducing the risk of complications.
4. Post-operatively, the cage's design promotes bone growth, leading to successful fusion and long-term stability.
5. The cage is also used in revision surgeries, where previous fusion attempts have failed, offering a reliable solution for complex cases.

The PEEK Interbody Fusion Cage has proven to be a versatile and effective tool in clinical applications, particularly in spinal fusion surgeries. Its ability to provide stability, promote bone growth, and offer clear imaging makes it a preferred choice for treating a range of spinal conditions.

Purchasing Guide

When purchasing the PEEK Interbody Fusion Cage, it is essential to consider factors such as product specifications, types, budget, and intended use to ensure the best fit for your clinical needs.

1. Product specifications, including size, material, and sterilization status, should be carefully reviewed to ensure compatibility with the intended surgical procedure.
2. The cage is available in various types, including cervical and lumbar versions, each designed to meet specific anatomical and functional requirements.
3. Budget considerations should include not only the initial purchase cost but also long-term factors such as shelf life and potential need for revision surgeries.
4. The intended use, whether for primary or revision surgeries, should guide the selection process, ensuring that the chosen cage meets the specific needs of the patient and the surgical team.

Purchasing the PEEK Interbody Fusion Cage requires careful consideration of various factors, including product specifications, types, budget, and intended use. By taking these into account, you can ensure that the chosen cage will meet your clinical needs and provide the best possible outcomes for your patients.

 Precautions

Proper handling and use of the PEEK Interbody Fusion Cage are crucial to ensure patient safety and optimal surgical outcomes. Key precautions include proper sterilization, accurate placement, and adherence to surgical protocols.

1. Ensure that the cage is properly sterilized before use, especially if opting for the non-sterile version, to prevent infections and other complications.
2. Accurate placement of the cage is essential for successful fusion. Use imaging techniques to guide placement and ensure optimal positioning.
3. Adhere to all surgical protocols and guidelines, including proper handling of the cage and associated instruments, to minimize the risk of complications.
4. Monitor the patient post-operatively for signs of infection, improper fusion, or other complications, and take appropriate action if any issues arise.
5. Ensure that all surgical team members are trained in the proper use and handling of the cage to prevent errors and ensure the best possible outcomes.

The PEEK Interbody Fusion Cage requires careful handling and adherence to surgical protocols to ensure patient safety and successful outcomes. By following these precautions, you can minimize risks and provide the best possible care for your patients.

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