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GALAXY™ Fixation



​​​ANATOMIC​AL  SITE​:Humerus, Elbow, Forearm, Wrist, Pelvis, Hip, Femur, Knee,  Tibia, Ankle


Galaxy fixation is a modular external fixation system for fracture treatments of lower and upper limbs.


  • Fast and easy assembly
  • Orthofix proven stability
  • Flexibility of use
  • MRI Conditional 1.5T and 3T only (More details are available on relevant Instructions For Use - PQGAL)
  • Sterile kits and components


  • Temporary and definitive fixation capability
  • Three different size clamps all with pin to bar/bar to bar flexibility
  • Specific anatomical units for elbow and shoulder
  • Three different diameter radiolucent rods with multiple lengths



The Galaxy Fixation System is intended to be used for bone stabilization in trauma and orthopedic procedures, both on adults and all pediatric subgroups excepts newborns as required. The indications for use include:

  • Open or closed fractures of the long bones
  • Vertically stable pelvic fractures or as a treatment adjunct for vertically unstable pelvic fractures
  • Infected and aseptic nonunions
  • Joint pathologies/injuries of upper and lower limb, such as:
    • Proximal humeral fractures
    • Intra-articular knee, ankle and wrist fractures
    • Delayed treatment of dislocated and stiff elbows
    • Chronic, persistent elbow joint instability
    • Acute elbow joint instability after complex ligament injuries
    • Unstable elbow fractures
    • Additional elbow stabilization of post-operative unstable internal fixation​​​


Galaxy External Fixation System is contraindicated for:

  • Patients with mental or physiological conditions who are unwilling or incapable of following postoperative care instructions
  • Patients with severe osteoporosis
  • Patients with severe, poorly controlled diabetes mellitus
  • Patients with compromised vascularity
  • Patients with previous infections
  • Patients with malignancy in the fracture area
  • Patients with neuromuscular deficit or any other conditions that could influence the healing process
  • Patients who are HIV positive
  • Patients with foreign body sensitivity where material sensitivity is suspected, tests should be made prior to implanting

Clinical References