The VERTEX MAX Reconstruction System received 510(k) clearance from the U.S. Food and Drug Administration in Dec. 2004 for laminar hook placement on the C1 - T3 vertebrae and for pedicle screw use ...

Medtronic recently announced it has received clearance from the FDA for expanded indications of its Vertex Reconstruction System. The new clearance for the Vertex family of products allows for ...

DUBLIN - Feb. 16, 2015 - Medtronic plc (MDT), today announced that it has received clearance from the U.S. Food and Drug Administration (FDA) for expanded indications of the VERTEX ® Reconstruction ...

Medtronic (Dublin) said that it has received clearance from the FDA for expanded indications of the Vertex Reconstruction System. The new clearance for the Vertex family of products allows for lateral ...

Medtronic, Inc. announced the United States launch of the VERTEX SELECT Reconstruction System Posted Screw Module which came during the 2010 Annual Meeting of the North American Spine Society ...

DUBLIN - Feb. 16, 2015 - Medtronic plc (MDT), today announced that it has received clearance from the U.S. Food and Drug Administration (FDA) for expanded indications of the VERTEX ® Reconstruction ...

DUBLIN - Feb. 16, 2015 - Medtronic plc (MDT), today announced that it has received clearance from the U.S. Food and Drug Administration (FDA) for expanded indications of the VERTEX ...