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Spine · Cervical

VERTELIFT-C Anterior cervical corpectomy cage

Vertebral body replacement for the cervical spine.

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VERTELIFT-C Anterior cervical corpectomy cage

Overview

After a cervical corpectomy the vertebral body is gone. The defect has to be bridged and held at the right height until the segment fuses. VERTELIFT-C is a titanium corpectomy cage that is inserted at its closed length and then lengthened in situ to the measured gap. One locking step fixes the chosen height.

Product group
Spine
System
Cervical
Anatomical region
Cervical spine
Material
Titanium
Manufacturer
NORMMED MEDİKAL SAN. VE TİC. A.Ş., Ankara
Intended purpose, contraindications, warnings and precautions are given in the instructions for use. Search the e-IFU

Design rationale

Distraction in situ

The cage enters the corpectomy defect closed, and the centre piece is then turned with the opener until the end pieces meet the adjacent vertebrae. Final height is therefore set against the real gap rather than a trial. A blue marking appears when the maximum distraction height has been reached.

Single-step locking

Once the position has been checked, the end pieces are locked to the centre piece with the lock screw fixer. Height is fixed in one step at the length the surgeon chose.

Graft space and endplate contact

A widened graft space allows the cage to be grafted before it is distracted in the defect. Angled upper and lower surfaces are designed to give full contact with the vertebral surface, which spreads load over the endplate. The contact faces carry teeth and a threaded surface.

Measured in situ

A length guide measures the defect from the posterior aspect of the endplates. The cage is chosen so that its closed length is shorter and its opened length longer than the defect, so it goes in without force and is then opened to bear on both endplates.

Indications

  • Anterior cervical corpectomy and fusion for patients with symptomatic, progressive cervical spinal stenosis and myelopathy
  • Removal of large osteophytes that compress the spinal cord and spinal nerves

Source: Normmed product catalogue.

Regulatory status

Families marked EU MDR are named on EU MDR certificates. The other spine families are CE-marked under the MDD and remain legally marketed under the MDR transition provisions while their MDR certification is ongoing.

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