Mortise Medical passes US FDA clearance for LigaMetrics Suture Anchor System in ligament surgery.
M2 EQUITYBITES-September 27, 2017-Mortise Medical passes US FDA clearance for LigaMetrics Suture Anchor System in ligament surgery
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Medical device company Mortise Medical reported on Tuesday the receipt of US FDA 510(k) clearance for its innovative LigaMetrics Suture Anchor System for precision in ligament and tendon surgery.
The company added that the Mortise Medical LigaMetrics Suture Anchor System is the first and only knotless suture anchor that provides precise, measured tension control of the suture repair construct as well as unmatched surgeon control for achieving optimal stabilisation to facilitate healing of injured ligaments and tendons.
Designed specifically for connecting to and locking suture tape that is attached either to soft tissue or attached to a conventional suture anchor, the surgical technique for the LigaMetrics Suture Anchor System is designed to place maximum control of the final repair construct in the hands of the surgeon, said the company.
According to the company, the LigaMetrics Suture Anchor is fully seated into the bone and then the Metrics Tensioner is engaged with the anchor and suture tape to apply measured, controlled tension to the repair construct. The stability and range of motion assessments can be conducted and further fine adjustments to tension can be made by the surgeon to optimize the quality of the repair.
Following optimal tension, the torque controlled locking feature of the LigaMetrics Suture Anchor is activated to lock the suture tape to the anchor, eliminating the need to for knot tying, concluded the company.
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|Publication:||M2 EquityBites (EQB)|
|Date:||Sep 27, 2017|
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