OrthoLimited
tlif peek cage instrument set
OrthoLimited

TLIF PEEK Cage Instrument Set

TLIF PEEK Cage Instrument Set β€” a orthopedic instrument from OrthoLimited, supplied to ISO 13485 standards for hospitals and distributors worldwide.

SKU
2200-08
MPN
2200-08
Brand
OrthoLimited
Manufactured by
OrthoLimited Inc.
Warehouse
EU
Availability
In stock
  • βœ“ CE marked
  • βœ“ ISO 13485
  • βœ“ Warranty included
  • βœ“ Worldwide shipping
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Regulatory: For professional surgical use only. Availability and certification vary by country; confirm local regulatory status before purchase or use.

Clinical overview

Product overview

TLIF PEEK Cage Instrument Set

TLIF (Transforaminal Lumbar Interbody Fusion) PEEK (Polyether Ether Ketone) cage instrument set is a surgical tool kit used in spinal fusion surgery to implant a PEEK cage into the intervertebral disc space through a minimally invasive approach. The TLIF PEEK cage is designed to provide structural support and promote fusion between the adjacent vertebral bodies while maintaining the natural disc height and alignment.

The TLIF PEEK cage instrument set typically includes various tools and instruments such as reamers, drills, curettes, and implant inserters that are used to prepare the disc space and insert the cage. The set may also include specialized instruments such as nerve retractors, nerve root hooks, and disc space spreaders to aid in the surgical procedure.

TLIF PEEK cages are available in different shapes and sizes to match the patient's anatomy, and they are typically implanted with bone graft material to facilitate fusion between the vertebral bodies. The use of a TLIF PEEK cage can help reduce the risk of complications associated with traditional open spinal fusion surgery, such as blood loss, muscle damage, and longer hospital stays.

Technical specifications

Engineering at a glance

Documentation, IFU and DOCs available on request β€” contact our sales team for the full regulatory file.

Model
2200-08

Documents & downloads

Regulatory paperwork & manuals

Pre-cleared documentation for this device. Full tender-pack originals are available on request.

Documents & downloads

Regulatory paperwork & manuals

This device's IFU, CE Declaration of Conformity, ISO 13485 certificate and (where applicable) FDA 510(k) clearance ship with the order. Reach out below for the pack ahead of purchase.

Get in touch

Need configuration help, certificates, or volume pricing?

Our clinical sales team will scope quantities, voltage, accessories and regulatory paperwork β€” usually within one business day.

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