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Hip & Knee · Total knee — GORDION

GORDION PS and CR cemented femoral components

Posterior-stabilised and cruciate-retaining femoral components, offered in A/P and M/L increments; CoCr.

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GORDION PS and CR cemented femoral components

Overview

A primary total knee needs a femoral component that fits the distal femur and influences how the knee behaves through flexion. GORDION femoral components are CoCr and cemented. The system is anterior-referencing and is implanted with the Total Knee System instrument set.

Product group
Hip & Knee
Anatomical region
Knee
Material
CoCr
Manufacturer
NORMMED MEDİKAL SAN. VE TİC. A.Ş., Ankara
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Design rationale

Size range and interchangeability

A/P and M/L size increments are designed to give a comprehensive femoral sizing solution. Femoral and tibial implant sizes are interchangeable. The tibial baseplate is therefore chosen for coverage of the proximal tibia rather than matched to the femoral size.

Single-radius femoral design

The femoral component has a single radius that stays constant in the coronal plane. It is designed to give an even contact area between the femoral component and the insert.

PS post and cam

In the PS version, the curved anterior post on the insert and the PS femoral cam are designed to reduce potential for impingement and polyethylene wear.

CR femoral component

The CR femoral component retains the posterior cruciate ligament and needs no intercondylar housing cut. Femoral preparation for CR is complete after the A/P and chamfer cuts.

One platform, one instrument set

GORDION has two femoral designs on one tibial platform. One instrument set prepares both versions. The PS box is cut last, so the choice between CR and PS can be made in the theatre.

Indications

  • Painful and restrictive knee joint disease caused by non-inflammatory degenerative disorders (osteoarthritis, traumatic arthritis or avascular necrosis), rheumatoid arthritis or post-traumatic arthritis
  • Advanced arthrosis that has not responded to conservative or arthroscopic measures
  • Pain with excessive loading or at rest
  • Increasing limitation of movement
  • Mild varus, valgus or flexion deformity in which the ligamentous structures can be restored to adequate function and balance

Source: Normmed product catalogue.

Regulatory status

These 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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