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Gamma Nail

  • 1100-06
  • CZMEDITECH
  • Stainless Steel / Titanium
  • CE/ISO:9001/ISO13485
  • FedEx. DHL.TNT.EMS.etc
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Product Description

Product operation details video

CZMEDITECH Gamma Nail

Introduction

The gamma nail or trochanteric nail is an osteosynthetic implant designed to treat proximal femoral fractures in the trochanter area with a closed intramedullary fixation method.


The gamma nail consists of a funnel-shaped intramedullary nail with slight bending to reflect proximal femoral diaphyseal trochanteric morphology, a large proximal opening, which features a sliding mechanism for a large femoral neck lag screw and small holes in the distal part enabling distal femoral locking of the implant .


Gamma nails come in different lengths, longer nails are designed to provide stability in intertrochanteric and subtrochanteric fractures with diaphyseal fracture extension .


Features & Benefits

Gamma Nail

Specification

CZMEDITECH
Material
Stainless steel/Titanium alloy
Certificate
CE,ISO13485
Diameter
9/10/11mm
Length
180/200/220/240/260/280mm
Other
Customizable
Delivery Way
DHL/UPS/FEDEX/TNT/ARAMAX/EMS
Delivery Time
3-7 days

Precautions

Gamma Nail Uses

  1. Comminuted fractures

  2. Segmental fractures

  3. Fractures with bone loss

  4. Proximal and distal fractures

  5. Subtrochanteric fractures

  6. Intertrochanteric fractures




Gamma Nail Contraindications

The physician’s education, training and professional judgement must be relied upon to choose the most appropriate device and treatment.


Conditions presenting an increased risk of failure include:

  1. Any active or suspected latent infection or marked local inflammation in or about the affected area.

  2. Compromised vascularity that would inhibit adequate blood supply to the fracture or the operative site.

  3. Bone stock compromised by disease, infection or prior implantation that can not provide adequate support and/or fixation of the devices.

  4. Material sensitivity, documented or suspected.

  5. Obesity. An overweight or obese patient can produce loads on the implant that can lead to failure of the fixation of the device or to failure of the device itself.

  6. Patients having inadequate tissue coverage over the operative site.

  7. Implant utilization that would interfere with anatomical structures or physiological performance.

  8. Any mental or neuromuscular disorder which would create an unacceptable risk of fixation failure or complications in postoperative care.

  9. Other medical or surgical conditions which would preclude the potential benefit of surgery.


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