clearance
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Spine
Nanovis Spine, LLC receives FDA 510(k) clearance of its FortiBridge cervical plating system designed to complement the FortiCore® cervical interbody fusion device platform
Nanovis Spine, LLC receives FDA 510(k) clearance of its FortiBridgeTM cervical plating system designed to complement the FortiCore® cervical interbody…
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FH Ortho Receives FDA 510(k) Clearance for Its CALCAnail® Orthopedic Arthrodesis Nail
CHICAGO–(Business Wire)–FH Ortho, maker of thoughtfully designed orthopedic devices and instruments for surgeons around the world, today announced it has…
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Hospitals
Rivanna Medical has Received FDA Clearance for Accuro™
CHARLOTTESVILLE, Va., Jun 01, 2015 (BUSINESS WIRE) — Rivanna Medical announced today that it has received FDA 510(k) clearance to market Accuro™,…
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Spine
Captiva Spine® Broadens Product Offering with 510(k) Clearance for CapLOX II™ Spinal System
Jupiter, FL, September 15, 2011 –(PR.com)– Captiva Spine, Inc., a medical device organization dedicated to developing and distributing spinal technologies in the US…
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Stryker Receives FDA 510(K) Clearance for Shapematch® Cutting Guides
Kalamazoo, Michigan – May 24, 2011 – Stryker Orthopaedics, a division of Stryker Corporation (NYSE:SYK), today announced that its ShapeMatch…
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Medyssey Spine Receives 510(k) Clearance for Its LP Cage(TM) Posterior Lumbar Interbody Fusion System
CHICAGO, April 13, 2011 /PRNewswire/ — Medyssey Co., Ltd., the parent company of Medyssey Spine, a spinal implant manufacturer focused on commercializing products…
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Medyssey Spine Receives FDA 510(k) Clearance for Zenius(TM) Thoracolumbar Spinal System in Titanium Alloy (Ti6AL-4V ELI)
LOS ANGELES, Aug. 25 /PRNewswire/ — South Korea-based Medyssey Co., Ltd. announced today that the Company has received 510(k) clearance from the U.S.…
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Bovie Medical Corporation Announces Clearance to Market Its BOSS™ Soft Tissue Coagulation Device
MELVILLE, N.Y.–(BUSINESS WIRE)–Bovie Medical Corporation (the “Company”) (NYSE-AMEX Symbol: BVX), a manufacturer and marketer of electrosurgical products, today announced the…
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FDA Schedules Public Meeting on Premarket Clearance Process for Medical Devices
FDA NEWS RELEASE For Immediate Release: Jan. 22, 2010 Media Inquiries: Peper Long, 301-796-4671, mary.long@fda.hhs.gov Consumer Inquiries: 888-INFO-FDA FDA Schedules Public…
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SpineWorks to Exhibit FixxSure Cross Link Technology at North American Spine Society Meeting
HUNTINGTON BEACH, Calif.--(Business Wire)--SpineWorks, a medical device company focused on developing technologies to help treat those with complex spine conditions,…
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