Medtronic Announces Approvminimally invasive tubular retractoral and Launch of Japan’s First DBM Bone Grafting Product for Spine and Orthopedic Procedures

DUBLIN and TOKYO – February 28, 2019 – Medtronic plc (NYSE:MDT) announced today the Japanese launch of the Grafton(TM) Demineralized Bone Matrix (DBM) bone grafting product for spine and orthopedic procedures. Grafton DBM is the first and only demineralized bone matrix product available in Japan, the world’s second largest market for spinal medical devices. Due to …

MCRA Assists with Pstabilization deviceremarket Approval of the M6-C Artificial Cervical Disc

WASHINGTON, March 7, 2019 /PRNewswire/ —  MCRA, LLC announced today its role in the successful Premarket Approval (PMA) application decision by the U.S. Food and Drug Administration (FDA) to approve the Orthofix M6-C™artificial cervical disc for the treatment of single level cervical disc degeneration. A next-generation artificial cervical disc, the M6-C disc developed by Spinal Kinetics LLC is …

Orthofix Announces FDA Approval of the M6-C Artificial Cervical Disc to Treat Patients with Cervical Dbest back surgeonsisc Degeneration

February 07, 2019  LEWISVILLE, Texas–(BUSINESS WIRE)–Orthofix Medical Inc. (NASDAQ:OFIX), a global medical device company focused on musculoskeletal products and therapies, today announced U.S. Food and Drug Administration (FDA) approval of the M6-C™ artificial cervical disc for patients suffering from cervical disc degeneration. The M6-C artificial cervical disc was developed by Spinal Kinetics, a company acquired by …

TranS1® Announces NICE Guidance for Approval of AxiaLIF® in the UK’s National Health System (NHSwolf spine)

WILMINGTON, N.C., Sept. 18, 2018 /PRNewswire/ — TranS1®, an innovator in spine technology development that pioneered the anterior retroperitoneal presacral approach utilizing the Apeek spinal fusionxiaLIF® System, announced today that the UK’s National Institute for Health and Care Excellence (NICE) published its Interventional Procedure Guidance recommendation for  transaxial interbody lumbosacral fusion for severe chronic low back pain.1 The guidance …

Medtronic lumbar disk herniationAnnounces FDA Approval of Infuse(TM) Bone Graft in New Spine Surgery Indications Using PEEK Interbody Implants

DUBLIN – April 30, 2018 – Medtronic plc (NYSE: MDT) today announced U.S. Food and Drug Administration (FDA) approval of Infuse(TM) Bone Graft in new spine surgery indications. InfuseBone Graft is now approved for use with additional spine implants made of polyetheretherketone (PEEK) in oblique lateral interbody fusion (OLIF 25(TM) and OLIF 51(TM)) and anterior lumbar …

CTL Wins FDA Approval for Seurat Universal Pedicle spine bonesScrew

DALLAS, TX / ACCESSWIRE / March 29, 2018 / CTL Medical Corporation, a Dallas-based medical device manufacturing and service company, has recently secured clearance and approval from the Food and Drug Administration to market its new SEURAT Universal Pedicle Screw System for the practice of spine fusion surgery. This is the second FDA clearance for the …

EIT Emerging Implant Technologies Announces 51spinal disc spacers0(k) Approval from the FDA for Full 3D Printed Cage Portfolio and Begins Commercialization in the U.S.

Emerging Implant Technologies GmbH (EIT), a German medical device manufacturer exclusively focused on creating innovative technologies for spinal application by utilizing additive manufacturing, announces that it has received full approval from thback pain operatione FDA to commercialize its spinal interbody product offerings for ALIF, TLIF, PLIF and Cervical procedures. EIT Cellular Titanium® is a porous …