By Elizabeth Hofheinz, M.P.H., M.Ed., August 30, 2019 “When it comes to stem cells and PRP, we wage a battle against the public’s perception of these treatments. “I wish patients wouldn’t take medical advice from their hairdresser/waitress/sports figures,” says one orthopedic surgeon. “Patients are talking to everyone about these treatments and are getting the idea …
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ATLANTA, Aug. 30, 2019 /PRNewswire/ — MiRus announces successful spine surgeries at several centers across the country using the MoRe® superalloy. MiRus had received FDA 510(k) clearance for the MoRe® based Europa™ Pedicle Screw System earlier this year. MoRe®, a proprietary molybdenum rhenium superalloy for medical implants, provides an unprecedented combination of strength, ductility, durability, and biological safety. The …
by Robert King | Aug 26, 2019 While the Trump administration wants hospitals to begin posting “shoppable” prices online starting next year, some hospitals are scrambling to figure out how they’ll be able to meet such a requirement. Some officials have complained that they do not have contracts automated in order to post such rates. Others say it …
August 28, 2019- Noblesville, IN- Nexxt Spine LLC, a pioneer in the design and manufacturing of innovative spinal solutions, is proud to release their Lordotic TLIF Oblique interbody into the market. Meticulously designed, Nexxt Spine’s newest creation is ready to take on transforaminal lumbar interbody fusion (TLIF), the most frequently performed procedure in the field. …
DALLAS, Aug. 28, 2019 /PRNewswire/ — 4WEB Medical, an orthopedic device company focused on developing innovative implants utilizing its proprietary Truss Implant Technology™, announced today that the company has received 510(k) clearance from the U.S. Food and Drug Administration (FDA) to market its Cervical Spine Truss System-Stand Alone (CSTS-SA) Interbody Fusion Device. Consistent with 4WEB’s existing product portfolio, CSTS-SA has …
STOCKHOLM – August 28, 2019. Karolinska Development’s portfolio company Promimic today announced that the company’s first spinal device utilizing HAnano Surface to improve osseointegration has now been 510(k) approved by the FDA. Promimic develops and markets products within nano-materials for innovative surface treatments and has developed the HAnano Surface that speeds up and improves the anchoring of …
COLLEYVILLE, Texas, Aug. 28, 2019 /PRNewswire/ — Bone Solutions Inc., announces a private label licensing agreement with Onkos Surgical covering OsteoCrete® technology — the first FDA (510k) cleared magnesium-based bone void filler in the orthopedic marketplace, designed to assist with bone repair and regeneration. Onkos intends to distribute and market the products under the GenVie™ brand name. OsteoCrete® is an injectable, …
SUSANNAH LUTHI / August 26, 2019 An Oklahoma state judge on Monday ruled that Johnson & Johnson fed the state’s opioid addiction crisis with aggressive marketing and sales, ordering the company to pay $572 million. The manufacturers’ “false, misleading and dangerous marketing campaigns have caused exponentially increasing rates of addiction overdose deaths and Neonatal Abstinence …
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