| Anatomical application |
Femoral, tibial, humeral, and other intramedullary nails are designed for specific bone anatomy and entry points. |
Confirm the nail is intended for the target bone, fracture zone, laterality, and planned entry approach. |
Malalignment, cortical perforation, soft-tissue irritation, or inability to achieve the planned locking configuration. |
| Common nail diameter range |
Typical adult planning ranges are approximately:
• Femur: 10–13 mm
• Tibia: 8–11 mm
• Humerus: 7–9 mm
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Measure the medullary canal using appropriate imaging and instrumentation. Confirm the implant’s available diameter increments and reaming requirements. |
Oversizing may cause insertion difficulty or cortical damage; undersizing may reduce stability and increase implant stress. |
| Distal and proximal nail geometry |
Nails differ in curvature, bend location, end shape, and locking-hole orientation. |
Compare the nail geometry with the patient’s anatomy, fracture level, deformity, and intended locking-screw trajectories. |
Loss of reduction, eccentric loading, screw-miss risk, or difficulty placing the nail at the correct depth. |
| Locking-screw diameter |
Common clinical ranges include approximately:
• Small-diameter systems: 3.5–4.0 mm
• Tibial and humeral systems: 4.0–5.0 mm
• Larger femoral systems: 5.0–6.5 mm
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Verify the exact screw diameter specified for each nail hole. Do not substitute a screw solely because its length or thread profile appears compatible. |
Inadequate fixation, screw deformation, hole damage, loss of locking security, or incompatibility with the targeting guide. |
| Locking-screw length |
Length is selected according to measured bone width, nail position, cortical thickness, and the required amount of bicortical purchase. |
Confirm the measurement technique and ensure the selected screw engages the intended cortices without excessive soft-tissue prominence. |
Insufficient purchase may reduce stability; excessive length may irritate soft tissue or endanger nearby structures. |
| Number of locking screws |
More screws and more locking points generally increase resistance to rotation and axial migration, but the appropriate construct depends on fracture pattern and bone quality. |
Follow the surgical plan and device-specific instructions for static, dynamic, or combination locking. |
Too few locking points may permit instability; unnecessary screws may increase operative time, tissue disruption, or stress concentration. |
| Locking-screw position |
Proximal and distal locking holes may be oriented in transverse, oblique, or multiplanar directions. |
Confirm the hole position relative to the fracture, joint, neurovascular structures, and the available targeting or freehand technique. |
Missed holes, joint penetration, neurovascular injury, inadequate control of length or rotation, or poor fracture stability. |
| Static versus dynamic locking |
Static locking controls length and rotation. Dynamic locking allows controlled axial motion when the nail and fracture pattern are suitable. |
Verify which holes are intended for static or dynamic use and whether the planned construct matches the fracture’s mechanical requirements. |
Premature shortening, excessive motion, delayed union, malrotation, or implant overload. |
| Thread and head compatibility |
Locking screws may differ in thread form, head design, recess geometry, and engagement mechanism. |
Use only screws identified as compatible with the selected nail system and confirm the required driver and insertion torque instructions. |
Cross-threading, stripping, incomplete seating, back-out, or inability to remove the screw safely. |
| Manufacturer load data |
Load capacity is device-specific and depends on nail diameter, screw diameter, hole location, construct configuration, test method, and boundary conditions. |
Obtain the current device-specific instructions for use and technical data. Record axial, bending, and fatigue limits only when the test method and configuration are clearly stated. |
Applying a generic load value to a different nail or screw configuration can result in inaccurate safety conclusions and implant failure. |
| Fatigue performance |
Fatigue strength is not represented by a single universal value for all intramedullary nails. It is affected by stress concentration, locking-hole design, screw configuration, and cyclic loading. |
Check the reported test conditions, cycle count, specimen configuration, failure criteria, and whether the data apply to the intended implant assembly. |
Overestimation of endurance may lead to fatigue fracture, screw breakage, or loss of fixation during delayed healing. |
| Material and imaging considerations |
Implants may be manufactured from metallic materials with different mechanical and imaging characteristics. |
Confirm the material, MRI conditions, artifact expectations, and any contraindications stated in the device documentation. |
Unexpected imaging artifacts, MRI-related hazards, corrosion concerns, or incorrect assumptions about mechanical behavior. |
| Final compatibility check |
Nail diameter, screw diameter, screw length, hole position, instruments, and load data all match the same approved implant system. |
Complete a documented preoperative and intraoperative verification using the current instructions for use and implant labels. |
Do not implant if any critical dimension or compatibility parameter remains unresolved. |