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Recon / Antegrade Femoral Nail - Stryker

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Trauma<br />

T2<br />

<strong>Recon</strong> / <strong>Antegrade</strong> <strong>Femoral</strong> <strong>Nail</strong><br />

<strong>Recon</strong> <strong>Nail</strong>ing System


T2<br />

<strong>Recon</strong> / <strong>Antegrade</strong> <strong>Femoral</strong> <strong>Nail</strong><br />

To complement the T2 <strong>Nail</strong>ing System, <strong>Stryker</strong><br />

Trauma has created a “new generation” femoral<br />

implant:<br />

The T2 <strong>Recon</strong> <strong>Nail</strong> offers surgeons two<br />

options – cannulated and solid lag screw insertion<br />

technique – while using a common T2 instrument<br />

platform.<br />

Unique design features for the <strong>Recon</strong> T2 <strong>Nail</strong> include:<br />

• Flexibility to switch from a standard antegrade<br />

femoral application to a recon application<br />

without changing the nail. This is achieved<br />

through a smart nail design that incorporates<br />

two locking configurations.


0mm<br />

0mm<br />

26mm<br />

70°<br />

125° CCD<br />

44mm<br />

10.5mm<br />

4° lateral valgus bend<br />

• Easy Trochanteric Tip Insertion due to a 4°<br />

valgus bend plus an antecurvature of approximately<br />

2000mm.<br />

• 5mm Fully Threaded Screw that targets the<br />

Lesser Trochanter due to a proximal oblique<br />

70° locking hole with 7° retroversion.<br />

• Insertion of two cannulated 6.5mm Lag<br />

Screws at a 125° CCD angle with a 10° lag<br />

screw anteversion. Secure Placement in Small<br />

<strong>Femoral</strong> Necks is achieved with a 10.5mm<br />

distance between the Lag Screws (17mm outer<br />

screw distance).<br />

• Cannulated 6.5mm Lag Screws for optimal<br />

insertion via a K-Wire. The Lag Screw has a<br />

special thread design for better grip, improved<br />

front cutting flutes for lower insertion torque<br />

and thinner flanks for less bone removal*.<br />

• Static or Dynamic distal locking options.<br />

• All T2 implants are made of type II anodized<br />

titanium alloy (Ti6Al4V) for enhanced biomechanical<br />

and biomedical performance.<br />

* test reports (310303CG4/5) on file at <strong>Stryker</strong>


The information presented in this brochure is intended to demonstrate a <strong>Stryker</strong> product. Always<br />

refer to the package insert, product label and/or user instructions before using any <strong>Stryker</strong> product.<br />

Surgeons must always rely on their own clinical judgment when deciding which products and<br />

techniques to use with their patients. Products may not be available in all markets. Product availability<br />

is subject to the regulatory or medical practices that govern individual markets. Please contact your<br />

<strong>Stryker</strong> representative if you have questions about the availability of <strong>Stryker</strong> products in your area.<br />

Products referenced with designation are trademarks of <strong>Stryker</strong>.<br />

Products referenced with ® designation are registered trademarks of <strong>Stryker</strong>.<br />

Literature Number: B1000025<br />

LOT C2505<br />

Copyright © 2005 <strong>Stryker</strong><br />

Printed in Germany<br />

<strong>Stryker</strong> Trauma GmbH<br />

Prof.-Küntscher-Strasse 1-5<br />

D-24232 Schönkirchen - Germany<br />

www.trauma.stryker.com

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