Ascendx Spine received the Spotlight award from the Southeast Medical Device Association for its presentation at the SEMDA conference. Because of its award-winning presentation, Ascendx has been asked to present at AvaMed 2013: The MedTech Conference this fall.
The device company recently received FDA 510(k) clearance for its minimally invasive devices for vertebral compression fractures, the Ascendx VCF Repair System and Ascendx Acu-Cut Vertebral Augmentation System.
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Cerebral, Spine Pre-Surgical Rehearsal Device Approved by FDA
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The device company recently received FDA 510(k) clearance for its minimally invasive devices for vertebral compression fractures, the Ascendx VCF Repair System and Ascendx Acu-Cut Vertebral Augmentation System.
More Articles on Devices:
Cerebral, Spine Pre-Surgical Rehearsal Device Approved by FDA
FDA Issues Class 1 Recall for DePuy Revision Knee Device
MAKO Surgical Names Christopher Marrus Senior VP of Sales