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subtalar joint stabilizer i extraosseous talotarsal stabilization-0

Subtalar Joint Stabilizer

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Subtalar joint stabilizer I (Extraosseous Talotarsal Stabilization)
Subtalar joint stabilizer I (Extraosseous Talotarsal Stabilization)

Subtalar joint stabilizer I (Extraosseous Talotarsal Stabilization)

   

Material: Titanium

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Product Description
Code Product Description Specification Material
74901801 Extraosseous Talotarsal Stabilization Ⅰ 8.0x15 T
74901901 Extraosseous Talotarsal Stabilization Ⅰ 9.0x15 T
74901101 Extraosseous Talotarsal Stabilization Ⅰ 10.0x15 T
74901111 Extraosseous Talotarsal Stabilization Ⅰ 11.0x15 T
74901121 Extraosseous Talotarsal Stabilization Ⅰ 12.0x15 T
The ‌CareFix Subtalar Joint Stabilizer‌ (Extraosseous Talotarsal Stabilization) is manufactured from ‌medical-grade titanium alloy‌ and available in ‌Type I, II, and III structural configurations‌. Designed to stabilize the subtalar joint for treating ‌flatfoot, posterior heel valgus deformities‌, and ‌subtalar joint dislocation/instability‌, this implant provides targeted correction while preserving joint function.
Indications
  • Flexible flatfoot‌ (pediatric, adolescent, or adult).
  • Flatfoot with navicular bone disorders‌.
  • Spastic or paralytic flatfoot‌ (e.g., posterior tibial tendon dysfunction).
  • Posterior heel valgus deformities‌.
  • Subtalar joint dislocation or instability‌.
Contraindications
  • Local soft tissue damage or defects‌ (insufficient tissue coverage at the implantation site).
  • Active or mixed infections‌ at the surgical site.
  • Poor bone quality‌ (osteoporosis, osteopenia, malignant tumors) compromising fixation.
  • Rigid flatfoot, vertical talus, subtalar/tarsal arthritis, or clubfoot deformities‌.
  • Hypersensitivity to implant materials‌.
  • Immunosuppressive disorders, severe hepatic/renal dysfunction, or uncontrolled diabetes‌.
  • Systemic psychiatric conditions‌.
  • Patient noncompliance with activity restrictions or postoperative care‌.
  • Children under 4 years old, elderly patients, or pregnant/breastfeeding women‌.
Features
  • ‌Titanium alloy biocompatibility‌: High strength, corrosion resistance, and long-term implant safety.
  • Minimally invasive procedure‌: Requires only a ‌1-3 cm incision‌, reducing tissue trauma.
  • Biomechanical correction: Restores natural hindfoot motion while preserving joint integrity for potential revision surgeries.
  • Self-contained design‌: No additional instruments or bone grafts required for implantation.

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