TLIF PEEK Cages 7×10×28 mm and 8×10×28 mm

The TLIF Cages PEEK 7×10×28 mm and 8×10×28 mm are spinal interbody implants intended for use in selected transforaminal lumbar interbody fusion (TLIF) procedures. TLIF is a surgical approach used to access the lumbar intervertebral disc space from a posterior and lateral direction. An appropriately selected interbody cage is placed in the prepared disc space to provide structural support and help maintain the space while bone fusion develops.

The suitability of these implants depends on their approved indications, design, patient anatomy, and the surgical technique selected by a qualified spine surgeon.

Purpose and Clinical Applications

Lumbar interbody cages are used in selected spinal fusion procedures where support between adjacent vertebral bodies is required. During a TLIF procedure, the surgeon prepares the disc space and places an implant according to the planned surgical technique. The implant's role is to support the interbody space and provide a structure for fusion when used as directed by the manufacturer.

These cages are intended for professional use in appropriate spinal surgery settings. The product title does not specify the exact spinal levels, approved patient indications, or whether supplemental fixation is required. These details must be confirmed through the manufacturer's instructions for use.

PEEK Material

The product title identifies the cages as PEEK, commonly referring to polyether ether ketone, a polymer used in certain spinal implant applications. PEEK implant designs are used in interbody fusion systems because of their material characteristics and suitability for specific medical device applications.

The exact PEEK formulation, radiographic markers, surface treatment, and manufacturing details are not specified in the title. These characteristics vary between implant systems and should be confirmed with the supplier. Do not assume that the cages contain radiopaque markers or a particular surface texture without product documentation.

Available Implant Sizes

The product title specifies two implant configurations:

• 7 × 10 × 28 mm

• 8 × 10 × 28 mm

The dimensions are presented in the order provided by the product title. The manufacturer should confirm which measurement represents height, width, and length, as well as the dimensional tolerances and available size options.

Selecting an appropriate cage size requires consideration of the patient's anatomy, the prepared disc space, implant positioning, and the surgeon's operative plan. The stated dimensions alone do not establish suitability for a particular patient or spinal level.

Implant Design and Surgical Compatibility

The cage's exact shape, footprint, insertion profile, lordotic angle, graft window, and surface features are not specified. These details can influence implant placement and compatibility with the intended procedure. Before purchasing, confirm the implant's design and the compatible insertion instruments, trial implants, and other required accessories.

The product title does not indicate whether the cages are supplied individually or as part of a larger kit. It also does not establish whether bone graft material or supplemental fixation components are included. Request a complete product inventory before ordering.

Handling, Sterility, and Storage

Spinal implants must be handled according to the manufacturer's instructions to avoid damage or contamination. Inspect the packaging and implant identification before use, and do not use a product with compromised packaging or visible damage. The sterility status, single-use designation, and storage requirements must be confirmed from the product labeling.

Implant preparation and surgical placement should follow the manufacturer's validated instructions and the facility's established protocols. Healthcare professionals should also verify the implant's traceability and documentation before clinical use.

Choosing the Correct TLIF Cage

When selecting TLIF PEEK Cages in 7 × 10 × 28 mm and 8 × 10 × 28 mm sizes, verify the dimensional orientation, implant geometry, approved indications, compatibility with surgical instruments, and any requirements for supplemental fixation. Confirm the manufacturer's material specifications, sterility status, and regulatory documentation applicable to the intended market.

Accurate product verification helps purchasing teams identify the correct implant configuration and supports appropriate planning by qualified spine surgery professionals.

Key Features

• PEEK lumbar interbody cage implants

• Designed for selected TLIF procedures

• Two stated size configurations

• 7 × 10 × 28 mm size option

• 8 × 10 × 28 mm size option

• Intended to provide structural support in the lumbar disc space

• Material identified as PEEK

• Exact dimensional orientation requires confirmation

• Implant geometry and lordotic angle are not specified

• Compatible instrumentation must be verified

• Sterility and packaging status require confirmation

• Use according to manufacturer instructions and approved indications

Product Specifications

Frequently Asked Questions

1. What are TLIF PEEK cages used for?

They are interbody implants intended for selected transforaminal lumbar interbody fusion procedures, where they provide structural support within the prepared lumbar disc space as fusion develops.

2. What sizes are available?

The product title specifies two sizes: 7 × 10 × 28 mm and 8 × 10 × 28 mm.

3. What does PEEK mean?

PEEK stands for polyether ether ketone, a polymer used in certain medical implant applications. The exact formulation and implant characteristics should be confirmed with the manufacturer.

4. Which dimension represents the height of the cage?

The product title lists the dimensions but does not define their order. Confirm the height, width, and length with the manufacturer before selecting an implant.

5. Are surgical instruments included with these TLIF cages?

The title does not confirm whether insertion tools, trial implants, or other instruments are included. Check the package inventory before ordering.

6. Are the TLIF PEEK cages supplied sterile?

The sterility status is not specified in the product title. Review the manufacturer's packaging and instructions for use before clinical preparation.

7. Are these cages suitable for every lumbar fusion procedure?

No. Suitability depends on the implant's approved indications, dimensions, design, patient anatomy, and the surgeon's clinical assessment.

8. What should be verified before purchasing?

Confirm the dimensions and their orientation, implant geometry, PEEK specifications, compatible instrumentation, supplemental fixation requirements, sterility status, and manufacturer documentation.