BioWorld MedTech

Sep. 19, 2012

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Aptus snags FDA 510(k) for thoracic-length HeliFX

Aptus Endosystems (Sunnyvale, California), a device company developing technology for endovascular aneurysm repair (EVAR), said it has received FDA 510(k) clearance for its thoracic-length HeliFX Aortic Securement System. Read More

Neovasc upbeat about Tiara preclinical study results

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International report: Medical Care Technologies signs MOU with Dragon Link

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Washington roundup: MHRA wants more frequent follow-up of St. Jude's Riatas

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Financings roundup: Health Care REIT in plan to offer up to 22 million shares

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Agreements/contracts: Illumina to provide MiSeq to FDA for genome analysis

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HIT roundup: Consumers are beginning to comparison shop healthcare

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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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FDA approves somo-v ABUS system for dense breast tissue

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MDD's Oncology Extra

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