OEM Surgical Hospital Use InterZan Titanium Interlocking Nail for Femur Supplier, Factories

Product Features The integrated screws of InterZan provide a second point of fixation in the femoral head, and allow for mechanical compression through the implant which is actively maintained after instrument removal. This combination creates strong interfragmentary friction and increases construct stability to resist complications such as rotation and varus collapse. With compression actively maintained postoperatively using the integrated screws, InterZan is designed to reduce unnatural movement of the hip at the fracture site. The worm gear mechanism converts rotation to active compression while stabilizing the medial fragment. The head of the compression screw pushes medially against the nail and unloads stress forces off the lateral wall. Available sterile-packed

Product Description

What is Interzan Intramedullary nail?

Intramedullary nail is a surgical procedure for repairing fractures and maintaining their stability. The most common bones fixed in this way are the thigh, tibia, hip joint, and upper arm. A permanent nail or rod is placed at the center of the bone. It will help you put weight on the bones.

It consists of Femoral Nail, lag Screw, compression screw, end cap, locking bolt.

Indications & Clinical Application

The InterZan Femoral Nail is indicated for fractures of the femur including simple shaft fractures, comminuted shaft fractures, spiral shaft fractures, long oblique shaft fractures and segmental shaft fractures; subtrochanteric fractures; intertrochanteric fractures; ipsilateral femoral shaft/neck fractures; intracapsular fractures; nonunions and malunions; polytrauma and multiple fractures; prophylactic nailing of impending pathologic fractures; reconstruction, following tumor resection and grafting; bone lengthening and shortening.
Mechanical Advantage: Preloaded Cannulated Set Screw allows for creation of a fixed angle device or facilitates postoperative sliding. The integrated compression screw and lag screw thread together to generate push/pull forces that hold compression after instruments are removed and eliminate Z-effect.

Product Specifications & Component Details

InterZan Femur Intramedullary Nailbb14875e Φ9.0 x 180 mm, Φ9.0 x 200 mm, Φ9.0 x 240 mm
Φ10.0 x 180 mm, Φ10.0 x 200 mm, Φ10.0 x 240 mm
Φ11.0 x 180 mm, Φ11.0 x 200 mm, Φ11.0 x 240 mm
Φ12.0 x 180 mm, Φ12.0 x 200 mm, Φ12.0 x 240 mm
InterZan Lag ScrewInterZan Femoral Nail2480 Φ11.0 x 70 mm, Φ11.0 x 75 mm, Φ11.0 x 80 mm, Φ11.0 x 85 mm
Φ11.0 x 90 mm, Φ11.0 x 95 mm, Φ11.0 x 100 mm, Φ11.0 x 105 mm
Φ11.0 x 110 mm, Φ11.0 x 115 mm, Φ11.0 x 120 mm
InterZan Compression Screw图片70 Φ7.0 x 65 mm, Φ7.0 x 70 mm, Φ7.0 x 75 mm, Φ7.0 x 80 mm
Φ7.0 x 85 mm, Φ7.0 x 90 mm, Φ7.0 x 95 mm, Φ7.0 x 100 mm
Φ7.0 x 105 mm, Φ7.0 x 110 mm, Φ7.0 x 115 mm
Locking Bolt图片71 Φ4.9 x 28 mm, Φ4.9 x 30 mm, Φ4.9 x 32 mm, Φ4.9 x 34 mm
Φ4.9 x 36 mm, Φ4.9 x 38 mm, Φ4.9 x 40 mm, Φ4.9 x 42 mm
Φ4.9 x 44 mm, Φ4.9 x 46 mm, Φ4.9 x 48 mm, Φ4.9 x 50 mm
Φ4.9 x 52 mm, Φ4.9 x 54 mm, Φ4.9 x 56 mm, Φ4.9 x 58 mm
InterZan End Cap图片72 +0 mm, +5 mm, +10 mm
Material Titanium Alloy
Surface Treatment Micro-arc Oxidation
Qualification ISO13485 / NMPA
Package Sterile Packaging 1pcs/package
MOQ 1 Pcs
Supply Ability 1000+ Pieces per Month

Frequently Asked Questions (FAQ)

What is the primary material used for the InterZan Nail System?
The system is manufactured using high-grade Titanium Alloy with a Micro-arc Oxidation surface treatment to enhance durability, biocompatibility, and biomechanical fixation.
How does the system prevent the "Z-effect"?
The integrated compression screw and lag screw thread together to generate coordinated push/pull forces. This mechanism maintains active compression after instruments are removed, effectively preventing screw migration and the Z-effect.
What clinical indications is this femoral nail designed for?
It is indicated for a wide range of femoral fractures including simple, comminuted, spiral, and segmental shaft fractures; subtrochanteric and intertrochanteric fractures; ipsilateral femoral shaft/neck fractures; intracapsular fractures; nonunions, malunions, and prophylactic nailing of pathologic fractures.
What are the packaging and sterilization standards?
Each implant comes in individual sterile packaging (1 piece per package), compliant with ISO13485 and NMPA medical device manufacturing qualifications.
What is the minimum order quantity (MOQ) and production capacity?
The MOQ is 1 piece, with a stable monthly supply ability exceeding 1,000 pieces per month to meet both urgent clinical needs and volume distribution.

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