Condition: Used Stryker TenXor External Fixation System 4936-9-900 Included in the Sale TenXor Clamps & Frame Components: 4936-0-018 – TenXor Connecting Clamp 4936-9-010 – TenXor Frame Component 4936-0-015 – TenXor Connecting Clamp 4936-0-021 – TenXor Connecting Clamp Schanz Screws: 4936-2-040 – Ø4.0 mm (x8) 4936-2-010 – Ø5.0 mm (x8) 4936-2-030 – Ø3.0 mm (x5) Carbon Fiber Rods & Wires: 5118-1-340 – Carbon Fiber Rod 340 mm (x7) 5101-2-450 – Smooth Wire Ø2.0 mm × 450 mm (x3) 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.
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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.
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The Stryker TenXor External Fixation System is a hybrid lower extremity fixation system and a member of the Hoffmann II product family, manufactured by Stryker Trauma AG (Geneva, Switzerland) under the Howmedica Osteonics brand. It is designed to address the surgical challenges associated with periarticular and intra-articular fractures of the lower extremity — in particular the proximal tibia, distal tibia, and tibial pilon — where conventional monolateral fixation cannot adequately stabilise juxta-articular fracture fragments without immobilising the adjacent joint.

The hybrid construct combines a periarticular tensioned fine-wire ring component with diaphyseal Apex half pins connected via carbon fibre or stainless steel rods, allowing stable fixation of small cancellous and articular bone fragments while maintaining early joint mobilisation and weight bearing. The fine-wire ring element interfaces with the Hoffmann II open ring system, accepting smooth wires up to Ø2.0 mm, and the diaphyseal component accepts standard Schanz screws in Ø3.0, Ø4.0, and Ø5.0 mm diameters.

Key Features:
System family: Hoffmann II (Stryker Howmedica Osteonics)
System type: Hybrid external fixation — ring + monolateral half pin construct
Primary indications: Proximal tibial plateau fractures (Schatzker V/VI), distal tibial pilon fractures, periarticular lower extremity fractures with soft tissue compromise
Wire diameters supported: Ø1.5 mm and Ø2.0 mm smooth Kirschner wires
Schanz screw diameters: Ø3.0 mm, Ø4.0 mm, Ø5.0 mm
Rod material: Carbon fibre (radiolucent) and stainless steel options
Carbon fibre rod diameter/length: Ø5 mm; lengths as per catalogue (e.g. 340 mm)
Ring type: Open rings — allow free wire placement without ring removal
Clamp system: Modular ring clamps and connecting clamps for multi-planar adjustment
Compatibility: Compatible with Hoffmann II ring system components and standard Apex half pins
Sterilisation: Autoclavable; supplied in moulded sterilisation tray system
Material: Implant-grade stainless steel (screws, wires, clamps); anodised aluminium / carbon fibre (rods and handles)

Indications include temporary or definitive stabilisation of complex periarticular tibial fractures, open fractures where soft tissue injury precludes internal fixation, fractures in polytrauma patients requiring damage-control orthopaedics, and cases requiring early joint mobilisation to support cartilage regeneration and functional recovery.

Note: Carbon fibre connecting rods are single-use items and must not be bent. Always refer to the current Stryker package insert and operative technique guide before clinical use.

Stryker TenXor External Fixation System product brochure — hybrid system for lower extremity, features and ordering information: Download PDF