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  3. STRATAFIX Symmetric PDS Plus Knotless Tissue Control Device

STRATAFIX Symmetric PDS Plus Knotless Tissue Control Device

STRATAFIX Symmetric PDS Plus Knotless Tissue Control Device

STRATAFIX Symmetric PDS Plus Knotless Tissue Control Device is an antibacterial (polydioxanone) monofilament, synthetic absorbable device prepared from the polyester, poly (p-dioxanone.)1 The device contains IRGACARE* MP (triclosan), a broad spectrum antibacterial agent, at no more than 2360 μg/m.1 STRATAFIX Symmetric PDS Plus Devices are indicated for general soft tissue approximation where use of an absorbable suture is appropriate.1 STRATAFIX Symmetric PDS Plus Device, being absorbable, is not to be used where prolonged (beyond six weeks) approximation of tissue under stress is required and is not to be used in conjunction with prosthetic devices (i.e. heart valves or synthetic grafts.)1 STRATAFIX Symmetric PDS Plus Device should not be used in patients with known allergic reactions to IRGACARE* MP (triclosan.)1

Instructions for Use

Instructions for use are found in the information that accompanied the product packaging.

STRATAFIX™ Symmetric PDS™ Plus

IMAGES

STRATAFIX™ Symmetric PDS™ Plus
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Related Procedures

Total Hip Arthroplasty
Total Hip Arthroplasty
Total Knee Arthroplasty
Total Knee Arthroplasty

References

* Registered Trademark of BASF Group

1. Ethicon, Inc. STRATAFIX Symmetric PDS Plus Knotless Tissue Control Device, Instructions For Use. 
 

© Johnson & Johnson Medical N.V., Belgium 2018-2019.
This site is published by Johnson & Johnson Medical N.V., Belgium which is solely responsible for its contents and is intended for EMEA audiences only. This site is intended for Healthcare Professionals. If you are a patient, it is important that you discuss information about the benefits and risks of products with your doctor.
Last updated February 22, 2019. The third-party trademarks used herein are trademarks of their respective owners. Data and usage fees may apply. See your carrier for more information.
*As of March 2017, per internal research conducted by Ethicon.
Please refer always to the Instructions for Use / Package Insert that come with the device for the most current and complete instructions.

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