Home » FDA CLEARS MICRUS ENDOVASCULAR'S BRAIN SURGERY DEVICE
FDA CLEARS MICRUS ENDOVASCULAR'S BRAIN SURGERY DEVICE
May 11, 2006
Thursday, Micrus Endovascular Corp. said the FDA cleared its Watusi guidewire platform a device used in brain surgery. Micrus
plans to start selling the product immediately in the U.S.
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