Condition: Used Stryker Stanmore METS Modular Tibial Femoral Trial Implants – Complete Set
Complete modular trial implant set. Please refer to images for exact contents and condition.
Included in the Set Tibial: Plateau Plates tmktp/Std20 tmktp/Std15 tmktp/Std10 tmktp/Std5 tmktp/Sm5 tmktp/Sm10 tmktp/Sm15 tmktp/Sm20 Femoral: Plateau Plates tmkfp/Std20 tmkfp/Std15 tmkfp/Std10 tmkfp/Std5 tmkfp/Sm5 tmkfp/Sm10 tmkfp/Sm15 tmkfp/Sm20 Principle Shafts tmfshft/135 tmfshft/120 tmfshft/105 tmfshft/90 tmfshft/75 tmfshft/60 tmfshft/45 Femoral Knee Components tmptfc/RSm – Right Small tmptfc/LSm – Left Small tmptfc/RStd – Right Standard tmptfc/LStd – Left Standard Tibial: Rotating Hinges (Metal Casing) tmkrhm/StdLg tmkrhm/SmLg tmkrhm/StdSt tmkrhm/SmSt Tibial: Fixed Hinges tmkfh/SmLg tmkfh/StdLg tmkfh/SmSt tmkhf/StdSt Tibial: Rotating Hinges (Polyethylene) tmkrhp/Sm tmkrhp/Std Important Regulatory Notice
The sale of this item may be subject to regulation by the U.S. Food and Drug Administration (FDA) and state and local regulatory agencies.
If applicable, do not purchase this item unless you are an authorised purchaser. Verification may be required prior to dispatch.
Buyer Responsibility
Any commissioning, calibration, certification, and validation required prior to clinical use is the sole responsibility of the buyer.
Disclaimer
Regardless of the origin of the equipment or any identification appearing upon it, this equipment is not certified or recommended by the seller for any specific use.
The purchaser agrees that the seller shall not be held responsible or liable for any injuries or damages, whether incidental or consequential, associated with the use of this equipment.
By purchasing this item, the buyer acknowledges and agrees to these terms.

The Stanmore METS (Modular Endoprosthetic Tumour System) is a modular titanium endoprosthetic system designed by Stanmore Implants Worldwide (now part of Stryker) for the reconstruction of large bone defects, typically following tumour resection or failed arthroplasty. Introduced in 2001, the METS system has since expanded to cover the proximal femur, distal femur, total femur, proximal tibia, proximal humerus, and pelvis.

The METS Distal Femur system was developed from experience gained from more than 1,500 custom-made distal femoral replacements. It uses the SMILES knee, which offers three tibial configurations — rotating hinge polyethylene, rotating hinge metal casing (suitable for extra-articular resection), and a fixed hinge for markedly unstable or deformed knees.

Individual components are connected via precision-made interlocking taper junctions, allowing rapid and reliable intraoperative assembly. Femoral shafts are sized in 15mm increments to match the resected bone site, and a range of collar diameters accommodates varying femoral cross-sections.

Indications for Use:
- Primary bone tumours of the distal femur
- Failed joint replacements
- Failed massive allografts
- Failed massive endoprosthetic replacements
- Severe trauma requiring distal femoral reconstruction
- Revision arthroplasty with significant bone loss

Key Specifications:
System Type: Modular Endoprosthetic Tumour System (METS)
Application: Distal femoral replacement / limb salvage
Minimum Resection (Distal Femur): 76mm
Maximum Resection (Distal Femur): 263mm
Shaft Sizing Increments: 15mm
Knee Options: Rotating hinge (polyethylene), rotating hinge (metal casing), fixed hinge
Collar Sizes: Range of diameters to match femoral cross-section
Stem Options: Curved cemented stems in multiple diameters and lengths
Material: Titanium alloy
Trial Components: Anodised blue, labelled 'TRIAL COMPONENT DO NOT IMPLANT'
Regulatory: CE marked; distributed by Stryker
Manufacturer: Stanmore Implants Worldwide Ltd (Stryker), Elstree, UK

Note: These are surgical trial/instrument components for intraoperative sizing and are not implantable devices. For full product information, refer to the Stanmore Implants / Stryker website.