510 (k) clearance
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Vertera Spine Announces FDA Clearance of the First Surface Porous PEEK Interbody Fusion Device
ATLANTA, Oct. 6, 2015 /PRNewswire/ — Vertera Spine, a developer of medical devices with advanced functional surface technologies for spine applications, today announced…
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Hospitals
FDA: IDE review times reduced by nearly a year
By Fink Densford The FDA released a report detailing improvements in clearing medical devices, stating it reduced investigational device exemption…
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Hospitals
VEXIM Initiates International Clinical Study
Toulouse, 4th June 2015 – VEXIM (FR0011072602 – ALVXM / EligiblePEA-PME), a medical device company specializing in the minimally invasive treatment of vertebral fractures, today announced the initiation of a…
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Hospitals
Enhanced complex spine portfolio
Leesburg, Virginia – K2M Group Holdings Inc. officials announced the company has received 510(k) clearance from the U.S. Food and Drug Administration…
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Hospitals
Stryker Spine Receives FDA Clearance for New Lumbar Plating System
ALLENDALE, N.J., March 25, 2015 /PRNewswire/ — Stryker Corporation’s Spine Division announced today that it has received 510(k) clearance from the U.S.…
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