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Not all products are registered and approved for sale in all countries or regions. Indications of use may also vary by country and region. Please contact your country representative for product availability and information. Product images are for reference only.

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  • Home
  • Spine Surgery
  • Thoracolumbar Stabilization
  • Interbody Fusion Devices
  • PROSPACE® 3D Oblique

Product Picture Web Enlargement-PROSPACE® 3D Oblique
Product Picture CW Enlargement-PROSPACE® 3D Oblique
Product Picture Web Enlargement-PROSPACE® 3D Oblique
Product Picture Web Enlargement-PROSPACE® 3D Oblique
Product Picture CW Enlargement-PROSPACE® 3D Oblique

PROSPACE® 3D Oblique
Transforaminal Lumbar Interbody Device

Intendend Use

  • Stabilization of the lumbar and thoracic spine through transforaminal approach, monosegmental and multisegmental.
  • Always use PROSPACE® 3D Oblique in conjunction with an internal fixator.
  • PROSPACE® 3D Oblique can be implanted through an open or minimally invasive transforaminal access (Oblique TLIF technique).

 

Implant Design

  • Solid frame without sharp edges for biomechanical stability and smooth insertion into the disc space minimizing the risk to injure surrounding soft tissue.
  • Open porous structure designed to provide primary and secondary stability.
  • The implant’s anatomical endplate design provides a good contact area between implant and vertebral endplates whilst allowing addition of bone material to enable bone growth through the center of the implant.
  • Bulleted nose for smooth insertion into the disc space.
  • Screw thread interface allows a firm connection to inserter.
  • Interlaced angle respecting an implant positioning 30° from the sagittal plane.
  • Good visibility in X-ray to localize implant positioning.[1], [2]
Read more

References

[1] Usability-Test, Usability Validation of AESCULAP® PROSPACE® 3D Oblique Cages, Tubingen, 2019. The usability of the AESCULAP® 3D Cage System PROSPACE® 3D Oblique was tested in April 2019, in a cadaver workshop with six independent test persons as intended users (surgeons specialized in spinal surgery or comparable fields). Parameters such as implant visibility under x-ray control, mechanical stability of the implant / instrument interface and implant surface evaluation in terms of tissue injury risk were tested among others. Acceptance criteria were fulfilled for all the above-mentioned parameters. All test users confirmed the absence of critical features that must be improved prior to clinical use. [2] Rehnitz, Christoph, PD Dr. med. Radiological image evaluation of AESCULAP® interbody fusion devices, Heidelberg, 2019. CT and X-ray visualization of different AESCULAP® interbody fusion cages (full titanium, porous Ti6Al4V and PLASMAPOREXP® cages) was tested in a cadaver setup. A radiologist evaluated the implant visibility and the presence of artefacts that may limit the visualization of adjacent structures. Visualization and assessment of implant position was achieved in X-ray and CT for all tested cages. Minor artefacts were visible in CT reconstructions in the surrounding of porous Ti6Al4V and full titanium implants. Porous Ti6Al4V implants showed slightly fewer artefacts in CT in comparison to full titanium implants. The minor artefacts observed did not limit the assessment of the surrounding anatomical structures.