The LCP Posteromedial Proximal Tibial Plate 3.5 mm (3–10 Holes) with LCP Screws – 70 pcs is an orthopedic implant system designed for selected fractures involving the proximal tibia. The proximal tibia forms the upper portion of the shinbone and contributes to the knee joint. Fractures in this region may involve the tibial plateau, metaphysis, or surrounding supporting structures and can require carefully planned fixation to restore alignment and maintain stability during healing.

The posteromedial plate configuration is intended for placement along the posteromedial aspect of the proximal tibia when indicated by the fracture pattern. It may be considered as part of a fixation strategy for fractures with a posteromedial fragment or other injury configurations requiring support from this direction. The appropriate implant and surgical approach must be determined by a qualified orthopedic surgeon following assessment of the fracture and relevant imaging.

Locking Compression Plate Technology

The locking compression plate (LCP) design uses specially engineered plate holes that can accommodate compatible locking screws. When correctly engaged, locking screws form a fixed-angle connection with the plate, helping maintain the planned relationship between the implant and screws. Depending on the specific plate design, compatible conventional screws may also be permitted for particular fixation techniques.

Fixed-angle fixation can be useful in selected periarticular fractures, where maintaining screw orientation and supporting smaller bone fragments are important considerations. The actual stability achieved depends on the implant design, bone quality, screw placement, fracture reduction, and the surgeon's technique. The 3.5 mm designation generally refers to the nominal screw system size, not necessarily the plate thickness.

Multiple Hole Configurations for Surgical Planning

This proximal tibial plate system includes configurations ranging from 3 to 10 holes. Different plate lengths and hole arrangements allow the surgical team to select an option appropriate for the fracture location, available bone stock, and required distribution of fixation points.

A shorter plate may be suitable for some fracture patterns, while a longer configuration may provide additional fixation positions when needed. The final selection depends on anatomical considerations and the manufacturer's approved surgical technique. Plate dimensions, contour, hole arrangement, and screw trajectories should be confirmed using the relevant product documentation rather than inferred from the product name alone.

LCP Screws and Fixation Compatibility

The 70-piece set is specified as including LCP screws. These screws are intended to work with the compatible plate system, subject to verification of the manufacturer's specifications. Screw diameter, length, thread design, and locking interface must match the plate and intended surgical application.

Appropriate screw selection helps the surgeon construct a fixation assembly suited to the fracture. Screw length and placement must be carefully assessed to avoid unwanted penetration into the knee joint or surrounding structures. The exact quantities and sizes of screws supplied in this set should be confirmed with the supplier before purchase.

Orthopedic Applications and Clinical Usability

The LCP posteromedial proximal tibial plate may be used in selected proximal tibial fracture fixation procedures where posteromedial support is required. Its intended role is to help maintain fracture reduction and provide structural fixation while the bone heals. It may also form part of a broader fixation construct when multiple fracture fragments or additional anatomical considerations require more than one plate.

This system is intended for professional orthopedic use in an appropriately equipped surgical environment. Successful application requires suitable fracture reduction, correct implant positioning, compatible screws, and compliance with the manufacturer's instructions for use.

Instrument Care, Sterilization, and Durability

Implant plates and screws must be handled according to their labeled sterile status and manufacturer instructions. Components supplied as sterile should be checked for package integrity and expiration information where applicable. Any reusable instruments included in an orthopedic set require validated cleaning, inspection, and sterilization procedures. Single-use implant components must not be reused or reprocessed unless specifically authorized by the manufacturer.

Material composition, surface treatment, mechanical properties, and implant longevity depend on the exact product specifications. Before procurement, verify the plate material, dimensions, screw compatibility, set contents, regulatory documentation, and approved indications. These checks help ensure that the selected orthopedic fixation system meets the clinical and institutional requirements for its intended use.

Key Features

• LCP posteromedial proximal tibial plate for selected orthopedic fracture fixation procedures

• Designed for the posteromedial aspect of the proximal tibia

• 3.5 mm nominal screw system

• Plate configurations ranging from 3 to 10 holes

• 70-piece set specified with compatible LCP screws

• Locking compression plate technology for fixed-angle screw fixation

• Supports fixation planning for selected proximal tibial and posteromedial fracture patterns

• Multiple plate configurations for different anatomical and fixation requirements

• Screw compatibility and dimensions should be verified with the manufacturer

• Intended for use by qualified orthopedic professionals

• Requires handling and sterilization in accordance with manufacturer instructions

• Suitable for orthopedic implant procurement after confirmation of specifications and set contents

Product Specifications

Frequently Asked Questions

1. What is an LCP posteromedial proximal tibial plate used for?

It is designed for fixation of selected fractures involving the proximal tibia when support along the posteromedial aspect is required. The surgeon determines its suitability according to the fracture pattern, imaging findings, and implant specifications.

2. What does 3.5 mm mean for a proximal tibial plate?

The 3.5 mm designation generally identifies the nominal screw system size associated with the plate. It does not necessarily represent the plate thickness. The exact compatible screw specifications should be confirmed with the manufacturer.

3. What do the 3–10 hole options mean?

The range indicates that different plate configurations are available with 3 to 10 holes. These options provide flexibility in plate length and fixation-point selection according to the anatomical requirements and surgical plan.

4. Why is a posteromedial plate used for proximal tibial fractures?

A posteromedial plate can provide support to selected fracture fragments located on the posteromedial side of the proximal tibia. Its use depends on the fracture configuration and the surgeon's assessment of the required fixation strategy.

5. Does the 70-piece set include LCP screws?

The product title specifies that LCP screws are included. However, the exact screw sizes, quantities, and distribution of the 70 components should be confirmed through the supplier's packing list.

6. Are LCP screws interchangeable between different plate systems?

Not necessarily. Compatibility depends on the screw diameter, thread design, locking interface, and the manufacturer's specifications. Only screws approved for the specific plate system should be used.

7. What material is the LCP posteromedial proximal tibial plate made from?

The material is not identified in the supplied product title. Confirm whether the plate and screws are manufactured from titanium alloy, stainless steel, or another specified implant material before purchasing.

8. How should the plate and screws be sterilized?

Follow the manufacturer's instructions for the implant's labeled sterile status and any reusable instruments supplied with the system. Reusable instruments require validated cleaning and sterilization, while single-use components must not be reused unless explicitly authorized.