OrthoLimited
reversed femoral nail
OrthoLimited

Reversed Femoral Nail

Reversed Femoral Nail β€” a intramedullary nail from OrthoLimited, supplied to ISO 13485 standards for hospitals and distributors worldwide.

SKU
1100-04
MPN
1100-04
Brand
OrthoLimited
Manufactured by
OrthoLimited Inc.
Warehouse
EU
Availability
In stock
  • βœ“ CE marked
  • βœ“ ISO 13485
  • βœ“ Warranty included
  • βœ“ Worldwide shipping
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Regulatory: For professional surgical use only. Availability and certification vary by country; confirm local regulatory status before purchase or use.

Clinical overview

Product overview

OrthoLimited Reversed Femoral Nail

Introduction

The incidence of fractures in the proximal femoral area has risen with the increasing numbers of elderly persons with osteoporosis and traffic accidents in young adults.

Fractures about the trochanteric area are classified according to the Orthopaedic Trauma Association classification system as AO/OTA 31-A, which delineates them as extracapsular fractures of the hip. These fractures are subdivided into groups A1, A2 and A3. A1 fractures are simple, two part fractures, whereas A2 fractures have multiple fragments. A3 fractures include reverse oblique and transverse fracture patterns.

There are two main types of implant available for the treatment of these fractures, namely, extramedullary and intramedullary implants [1–3]. Although the most widely used extramedullary implant is the dynamic hip screw, which consists of a sliding neck screw connected to a plate in the lateral femoral cortex, most authors have reported that this device is not suitable for AO/OTA 31-A3 reverse oblique or transverse fractures due to high incidence of fixation failures. Thus, the treatment of these unstable trochanteric femoral fractures is still challenging, and clinical reports regarding intramedullary hip nailing for reverse obliquity intertrochanteric fractures are few in number.

Technical specifications

Engineering at a glance

Documentation, IFU and DOCs available on request β€” contact our sales team for the full regulatory file.

Model
1100-04
Material
Stainless Steel / Titanium
Certification
CE, ISO 9001, ISO 13485

Documents & downloads

Regulatory paperwork & manuals

Pre-cleared documentation for this device. Full tender-pack originals are available on request.

Documents & downloads

Regulatory paperwork & manuals

This device's IFU, CE Declaration of Conformity, ISO 13485 certificate and (where applicable) FDA 510(k) clearance ship with the order. Reach out below for the pack ahead of purchase.

Get in touch

Need configuration help, certificates, or volume pricing?

Our clinical sales team will scope quantities, voltage, accessories and regulatory paperwork β€” usually within one business day.

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