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Monthly Archives: January, 2009

Stereotaxis first CTO crossing procedure received FDA approval

Stereotaxis, Inc. announced the first crossing of a chronic total occlusion using the RF PowerAssert(TM) magnetic guidewire cleared by the U.S. Food and Drug...

Lab-on-chip traces circulating tumor cells

Imagine a medical laboratory performing a genetic test to detect metastasis from blood in a breast cancer patient. Shrink this laboratory down to an...

Integra LifeSciences Launches a Series of PEEK-Optima(R) Interbody Spinal Implants

Integra LifeSciences Holdings Corporation (Nasdaq:IART) announced today the launch of a series of intervertebral body fusion devices (IBD), the Vu e-POD(TM) and Vu L-POD(TM)...

Integra LifeSciences acquired of Minnesota Scientific Inc

Integra LifeSciences Holdings Corporation announced that it has acquired Minnesota Scientific, Inc. (d/b/a Omni-Tract Surgical).  Omni-Tract Surgical, based in St. Paul, MN,...

Medegen Receives FDA Clearance for MaxGuard

Medegen, a leading innovator in infusion therapy products, today announced that it has received 510(k) clearance from the U.S. Food and Drug Administration (FDA)...

Covidien received 510(k) clearance to market Covidien SILS(TM)

Covidien, a leading global provider of healthcare products, announced that its Surgical Devices business unit has received 510(k) clearance from the U.S. Food and...

AGA Medical Receives Japanese Approval for AMPLATZER Duct Occluder

AGA Medical Corporation (“AGA Medical”) announced today that it received approval from the Japanese Ministry of Health, Labour and Welfare (MHLW) for its AMPLATZER®...

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