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 May 12, 2008 Volume 34 , Number 19 

Medtronic Recalls Certain Disposables Made With Contaminated Heparin
Safety concerns surrounding tainted lots of the anticoagulant drug heparin have moved more squarely into the device space with the “precautionary” recall of selected Medtronic products coated with the Carmeda BioActive surface.   READ MORE>>
Legal Issues Abound For Device Marketers In The Blogosphere
Tapping into the blogosphere could give medical device companies unprecedented access to patient and physician customers, but using blogs for marketing purposes carries a raft of legal responsibilities as well.    READ MORE>>
Senate Crafts Import Safety Bill, As Device Reps Prep For House Hearing
Sen. Ted Kennedy, D-Mass., is crafting a bill to strengthen FDA’s oversight of products manufactured overseas, including devices.    READ MORE>>
 
 
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  • Covidien Reports No Procedure Slowdown, Boosts Fiscal 2008 Guidance
     
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  • Boston Scientific Puts Its Own Stamp On New Line Of Pacemakers
     
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  • TranS1 Debuts “Least Invasive,” Two-Level Lumbar Spine Fusion System
     
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  • Financings In Brief
     
     
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  • Chart: FDA's April 2008 Clearances of 510(k)s
     
     
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  • Chart: FDA Recalls -- May 7, 2008

     
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  • Medtronic job cuts
     
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  • NuVasive buys biologic bone matrix product
     
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  • Boston Scientific/Medinol dispute
     
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  • Applera spins off Celera
     
     
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  • FDA Lifts Injunction On GE Surgical Unit’s Flagship Product
     
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  • FDA Task Force Takes Hard Look At Leachable Chemical In Medical Products
     
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  • Pre-Clinical Testing Issues Spark Questions From DES Manufacturers
     
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  • FDA News In Brief
     
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  • FDA Quality Systems Expert Shares Advice On CAPA Compliance
     
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  • Chart: FDA Warning Letters Released the Weeks of April 28 - May 5
     
     
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  • Coalition Asks Medicare Panel To Place PAD Screening Among Top Priorities
     
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  • House Panel Weighs Alternatives To DMEPOS Competitive Bidding Program
     
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  • CMS Denies Most New Code Requests For Durable Medical Equipment

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