The LCP Distal Humerus Medial Metaphyseal Plate – 3.5 mm, 4–10 Holes – 74 pcs, Titanium Grade 5 is an orthopedic fixation system intended for surgical management of selected distal humerus fractures. Designed for use in fracture fixation procedures, this plate system supports stabilization of the medial region of the distal humerus, where anatomical complexity and limited space can make implant positioning particularly important. Its locking compression plate design provides options for constructing a fixation assembly according to the fracture pattern, bone anatomy, and surgical treatment plan.

Distal Humerus Fracture Fixation

The distal humerus forms the lower portion of the upper-arm bone and contributes to the elbow joint. Fractures in this region may involve the metaphysis, extend toward the articular surface, or occur alongside other injuries affecting elbow stability. Depending on the fracture configuration, surgical fixation may require carefully positioned plates and compatible screws to maintain alignment and support bone healing.

The medial metaphyseal plate is intended to provide fixation along the medial aspect of the distal humerus. It may be considered for appropriate fracture patterns as part of an orthopedic trauma fixation strategy. Implant selection and positioning depend on the fracture classification, bone quality, available bone stock, and the surgeon's assessment of the required stability.

Locking Compression Plate Design

The locking compression plate (LCP) concept combines plate fixation with the option of using compatible locking screws and, where the system permits, conventional screws. Locking screws engage the plate holes to create a fixed-angle relationship between the screws and plate. This configuration can help maintain the planned fixation geometry and may be useful in selected fractures involving reduced bone quality or complex fracture patterns.

The 3.5 mm system designation identifies the nominal screw system size, rather than the plate thickness. Compatibility between the plate, screw diameter, screw head design, and instrumentation must be verified against the manufacturer's specifications before clinical use.

Grade 5 Titanium Construction

This plate system is specified as manufactured from Grade 5 titanium, commonly identified as Ti-6Al-4V. This titanium alloy is widely used in orthopedic implant manufacturing because of its favorable strength-to-weight characteristics and corrosion resistance. Its mechanical properties make it suitable for many applications in bone fixation when the implant is appropriately designed and manufactured.

Titanium construction can also be beneficial when a lightweight implant material is preferred. Actual mechanical performance, fatigue resistance, surface characteristics, and suitability for implantation depend on the verified material grade, manufacturing quality, and product-specific design.

Multiple Plate Configurations

The set includes plate configurations ranging from 4 to 10 holes, providing different options for fixation planning. Plate length and available screw positions influence how the implant can be positioned relative to the fracture and how fixation can be distributed across the bone. The appropriate configuration should be selected according to the anatomical requirements and the manufacturer's surgical technique.

The 74-piece set is intended to provide a collection of components for the specified plate system. The precise breakdown of plates, screws, and any supplementary instruments should be confirmed with the supplier before ordering, as the product title alone does not establish the complete inventory.

Clinical Usability, Sterilization, and Durability

The LCP distal humerus medial metaphyseal plate is intended for use by trained orthopedic professionals in an appropriately equipped surgical setting. Successful application requires proper fracture reduction, accurate implant positioning, compatible fixation components, and adherence to the manufacturer's instructions for use.

Reusable instruments supplied with an orthopedic fixation system must be cleaned, inspected, and sterilized according to their validated instructions. Implant components intended for single use must not be reused or reprocessed unless the manufacturer explicitly authorizes it. Titanium alloy offers corrosion resistance, but implant durability depends on correct application, loading conditions, patient factors, and compliance with the recommended surgical technique.

This 3.5 mm titanium plate system is a specialized option for orthopedic trauma inventory, hospital procurement, and surgical implant supply. Before purchase or clinical application, verify the exact plate dimensions, screw compatibility, set contents, regulatory documentation, and manufacturer-approved indications.

Key Features

• Product type: LCP distal humerus medial metaphyseal plate system

• Plate system size: 3.5 mm

• Hole configurations: 4–10 holes

• Set quantity: 74 pieces, subject to confirmation of the component breakdown

• Material: Titanium Grade 5, as specified in the product title

• Primary application: Selected distal humerus fracture fixation

• Anatomical focus: Medial metaphyseal region of the distal humerus

• Fixation concept: Locking compression plate technology

• Screw compatibility: Must be verified against the manufacturer's specifications

• Material benefits: Favorable strength-to-weight characteristics and corrosion resistance

• Clinical setting: Orthopedic trauma and fracture fixation procedures

• Processing requirements: Follow the manufacturer's instructions for cleaning, sterilization, and implant handling

Product Specifications

Frequently Asked Questions

1. What is an LCP distal humerus medial metaphyseal plate used for?

It is intended for fixation of selected fractures involving the distal humerus, particularly the medial metaphyseal region. The specific indication depends on the fracture pattern, implant design, and manufacturer's approved instructions.

2. What does 3.5 mm mean on a distal humerus plate?

The 3.5 mm designation generally refers to the nominal screw system size associated with the plate. It does not necessarily indicate the plate's thickness. Exact screw compatibility should be checked with the manufacturer.

3. What does the 4–10-hole configuration mean?

It indicates that the system includes plate options with hole counts ranging from 4 to 10. Different configurations provide choices for plate positioning and fixation planning according to the patient's anatomy and fracture characteristics.

4. What are the benefits of Grade 5 titanium orthopedic plates?

Grade 5 titanium alloy offers a favorable strength-to-weight ratio and corrosion resistance. Its suitability for a particular implant depends on the verified alloy composition, implant design, manufacturing standards, and intended clinical application.

5. What is included in the 74-piece distal humerus plate set?

The product title identifies a 74-piece set, but it does not specify the exact quantities of plates, screws, or supplementary components. Request a detailed packing list from the supplier to confirm the complete contents.

6. Are all 3.5 mm locking screws compatible with this plate?

No. A matching nominal size alone does not guarantee compatibility. Screw thread design, head geometry, locking mechanism, length, and manufacturer specifications must be checked before use.

7. Can the LCP distal humerus medial plate be used for every distal humerus fracture?

No. Plate selection depends on fracture location, fracture pattern, bone quality, available fixation points, and the patient's clinical circumstances. The treating orthopedic surgeon must determine the appropriate fixation method.

8. How should a titanium distal humerus plate be sterilized?

Implant components must be supplied and handled according to their labeled sterile status and manufacturer's instructions. Reusable instruments require validated cleaning and sterilization procedures. Implant components intended for single use should not be reused unless explicitly authorized by the manufacturer.