MiMedx Group's HydroFix Spine Shield device receives CE Mark

NewsGuard 100/100 Score

MiMedx Group, Inc. (OTC Bulletin Board: MDXG) announced today that the Company received the CE Mark for its HydroFix™ Spine Shield device and was certified for design, development, and production of post-surgical adhesion inhibiting barriers.  The HydroFix™ Spine Shield is indicated for use in specific locations as a cover of the spine to provide a plane of dissection during a revision surgery.  The proprietary, patented, and biocompatible polyvinyl alcohol polymer (PVA) membrane may reduce the risk of injury that may be associated with anterior vertebral surgeries. By covering the spine at the surgical repair site in anterior spine surgeries, HydroFix™ Spine Shield creates a plane of dissection for revision surgeries.

Dr. Rebeccah Brown, Executive VP of Product Development, said, "Anterior spine surgery patients can require revision surgeries, during which these patients are exposed to significant risk. The HydroFix™ Spine Shield was designed to create a plane of dissection to help minimize risk during the revision surgery."

Parker H. "Pete" Petit, Chairman, President and CEO, commented, "This is the first MiMedx Group product to receive a CE Mark for commercial sale.  The Company's strategy is focused on commercializing exciting new technologies, such as HydroFix™ Spine Shield, for orthopedic and other healthcare markets.  Our focused development efforts include a number of advanced technology products that we plan to introduce worldwide following their progression through the clinical and regulatory clearance and approval processes ."

The HydroFix™ Spine Shield is a permanent and biocompatible implant that is suitable as an adhesion inhibiting barrier or plane of dissection between anatomical structures. The proprietary and patented manufacturing process produces a product that is pliable, constructed in a single-layer and hydrophilic. The product may be trimmed and fitted easily at the time of use and is sutured into place.

The Company received notification from TUV Rheinland® that it obtained approval to apply the CE Mark on February 12, 2010.  HydroFix™ Spine Shield is not available in the United States.

SOURCE MiMedx Group, Inc.

Comments

The opinions expressed here are the views of the writer and do not necessarily reflect the views and opinions of News Medical.
Post a new comment
Post

While we only use edited and approved content for Azthena answers, it may on occasions provide incorrect responses. Please confirm any data provided with the related suppliers or authors. We do not provide medical advice, if you search for medical information you must always consult a medical professional before acting on any information provided.

Your questions, but not your email details will be shared with OpenAI and retained for 30 days in accordance with their privacy principles.

Please do not ask questions that use sensitive or confidential information.

Read the full Terms & Conditions.

You might also like...
New study reveals optimal drug sequencing for postmenopausal osteoporosis treatment