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Home » Newsletters » BioWorld MedTech

BioWorld MedTech

Nov. 11, 2013

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NewCo on the Go: ReShape to REDUCE obesity with new non-surgical device

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Medtronic gets FDA approval for Lead Integrity Alert software

Software developed by Medtronic (Minneapolis) will give the company greater insight into performance issues on defibrillator leads from competing firms when attached to one of the med-tech giant's devices. The company said that it received FDA approval of the Lead Integrity Alert (LIA) software to report performance issues on St. Jude's (St. Paul, Minnesota) Durata and Boston Scientific's (Natick, Massachusetts) Endotak defibrillator leads when connected to a Medtronic device. Read More

UK cautiously approves clot retrieval for stroke

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Washington roundup: Spinal Kinetics prevails over Synthes in hearing at CAFC

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Financings roundup: Incyte prices offering of convertible senior notes

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International report: Cerus to file regulatory submission in Canada

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Agreements/contracts: ViaFit teams with Ottobock for prosthetic arm fitting

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Med-Tech Notes

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People in the News

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Product Briefs

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MDD's Neurology Extra

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