Condition: Used Stanmore Implants METS Modular Endoprosthetic System Please refer to images for cosmetic condition and included components. Regulatory Notice
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The Stanmore METS (Modular Endoprosthetic Tumour System) is a modular titanium endoprosthetic system designed for the reconstruction of large bone defects, typically following tumour resection. Developed by Stanmore Implants Worldwide Ltd — a company with origins at the Royal National Orthopaedic Hospital, Stanmore — the METS system was introduced in 2001 and has since been used in thousands of procedures worldwide.

The system provides an off-the-shelf modular solution that can be adapted intraoperatively to suit each patient's anatomy, eliminating the delays associated with custom-made implants. Components connect via precision interlocking taper junctions for secure and reliable assembly.

Indications for use:
Primary bone tumours
Metastatic bone disease with impending or established pathological fracture
Failed joint replacements
Failed massive allografts or previous massive replacements
Complex skeletal reconstruction

Available system configurations:
Proximal Femur System
Distal Femur System
Total Femur System
Proximal Tibia System
Proximal Humerus System
Coned Hemi-Pelvis System

Key technical features:
Material: Titanium alloy construction
Resection range (Proximal Femur): 82mm minimum to 262mm maximum
Resection range (Distal Femur): 76mm minimum to 263mm maximum
Junction type: Interlocking taper junctions for modular assembly
Trials/instrumentation: Colour-coded anodised blue trial components in multiple stem lengths and body diameters
Head options: Range of modular metal and ceramic heads available
Trochanteric components: Anatomically shaped trochanter bodies with soft tissue reattachment provisions
Fixation: Cemented stem fixation options
Sterilisation: Instrumentation supplied in dedicated sterile trays for theatre use

The METS system's trial instrumentation (as presented here) is used intraoperatively to determine the correct implant sizing before the definitive prosthetic components are implanted. All trial components are clearly marked 'DO NOT IMPLANT'.