The Agile Nail is not designed or sold for any use except as indicated.

Use of the intramedullary nailing implant is contraindicated for patient with:

• General medical conditions not suitable for surgery;

• Active or suspected latent infections in the fracture area;

• Foreign body sensitivity (where material sensitivity is suspected, test should be made prior to implant insertion);

• Mental or physiological conditions who are unwilling or incapable of following postoperative care instructions;

• Pathological fractures without a diagnosis.

The AGILE NAIL™ is intended for insertion in the medullary canal of a femur for the alignment and the stabilization of fractures and for the correction
of deformities. It is indicated for the treatment of subtrochanteric fractures and of femoral shaft fractures, in pediatric patients, with the exception of
newborns and infants, and in adult patients with an appropriate medullary canal.

The indications include:

• prophylactic nailing of impending pathologic fractures;
• fixation of femurs that have been surgically prepared (osteotomy);
• nonunions and malunions;
• reconstruction following tumor resection and grafting and bone lengthening and shortening.

Minimally invasive (with a small diameter for the nails and the screws)

Early weight-bearing as tolerated by the patient and under surgeon discretion

Titanium alloy implants to avoid allergic reaction to nickel

10° proximal bending to facilitate the lateral insertion of the nail and to reduce the impact on the growth plate

Small proximal diameter of the nail for reduced invasiveness

Diameter from 7 up to 10mm

Titanium alloy implants

Procurvation design for easy insertion

Optimized and lean instrumentation

Jig with patented locking mechanism

Agile Nail Catalogue PDF

Agile Nail Operative Technique PDF

JuniOrtho Product Brochure PDF