The removal of the sanctions allowed the FDA today to approve four software upgrades to existing implantable devices and authorize a new supplier for a manufacturing component, Boston Scientific spokesman Paul Donovan said in an interview.But this slow-down was not without cost, as the device-maker has lost significant defibrillator and pacemaker product share to Medtronic and St. Jude Medical over the past twelve months.
Now the other 1,175 boat anchors in the form of lawsuits filed over Guidant's defibrillators remain.
-Wes
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