CytroFIX® Distal Fibula Medial Plate

What is CytroFIX® Distal Fibula Medial Plate?

CytroFIX distal fibula medial plate by INVAMED for ankle fractures requiring stable medial support and anatomical reduction. CE marked titanium locking plate.

How does CytroFIX® Distal Fibula Medial Plate work?

Buli yuanduan nei ce gangban, yongyugudingzhenji huai kokkyu.

What are the key features of CytroFIX® Distal Fibula Medial Plate?

• 板的形状反映了腓骨远端内侧的典型曲率，减少了术中过度弯曲的需要。
• 低调设计可最大程度地减少腓骨肌腱区域和周围结构的软组织刺激。
• 由医疗级钛（例如 Ti-6Al-4V ELI）制成，具有卓越的生物相容性和耐腐蚀性。
• 重量轻且耐用，支持更快的愈合并降低手术后种植体的可触及性。
• 多个孔阵列可容纳各种螺钉类型：标准皮质螺钉、锁定螺钉或可变角度锁定螺钉。
• 允许外科医生通过稳定、刚性的固定来解决不同的骨折类型。

Who manufactures CytroFIX® Distal Fibula Medial Plate?

CytroFIX® Distal Fibula Medial Plate is manufactured by INVAMED, a globally recognized medical device company headquartered in Ankara, Turkey. INVAMED holds over 100 international patents and exports CE marked devices to more than 80 countries. The company is ISO 13485 certified and FDA registered through Standard Technology Solutions, Inc. at One World Trade Center, New York.

What category does CytroFIX® Distal Fibula Medial Plate belong to?

CytroFIX® Distal Fibula Medial Plate is part of the Orthopedic & Trauma Solutions product portfolio by INVAMED. This category includes advanced medical devices designed for interventional procedures performed by healthcare professionals worldwide.

Which medical specialties use CytroFIX® Distal Fibula Medial Plate?

CytroFIX® Distal Fibula Medial Plate is used by specialists in Orthopedics & Trauma. These physicians rely on INVAMED devices for minimally invasive diagnostic and therapeutic procedures.

Is CytroFIX® Distal Fibula Medial Plate CE marked and FDA registered?

Yes. CytroFIX® Distal Fibula Medial Plate carries CE marking under EU MDR 2017/745 and is manufactured in ISO 13485 certified facilities. It is available in the U.S. market through FDA-registered Standard Technology Solutions, Inc.