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Tag: Medtronic

Medtronic Introduces MASTERGRAFT® Strip for Spinal Surgeries

Akillas | November 12, 2009 | 0 Comments
Medtronic Introduces MASTERGRAFT® Strip for Spinal Surgeries

SAN FRANCISCO – Nov. 11, 2009 – Medtronic, Inc. (NYSE: MDT) today announced the full U.S. market release of MASTERGRAFT® Strip – a new, highly flexible ceramic scaffold intended for use in combination with a patient’s own bone for fusing multiple levels of the posterolateral spine. The full market release was announced today at the [...]

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Medtronic, Inc. Launches Innovative Cement Delivery System for Kyphon® Balloon Kyphoplasty

Akillas | September 21, 2009 | 0 Comments
Medtronic, Inc. Launches Innovative Cement Delivery System for Kyphon® Balloon Kyphoplasty

MINNEAPOLIS – Sept. 21, 2009 – Medtronic, Inc. (NYSE:MDT), today announced the full U.S. launch of the KYPHON Cement Delivery System (CDS), adding an innovative bone cement delivery option to its extensive KYPHON Balloon Kyphoplasty product portfolio for the treatment of vertebral compression fractures (VCFs).

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Medtronic Reports First Quarter Revenue of $3.9 Billion

Akillas | August 27, 2009 | 0 Comments
Medtronic Reports First Quarter Revenue of $3.9 Billion

MINNEAPOLIS – August 25, 2009 – Medtronic, Inc. (NYSE:MDT) today announced financial results for its first quarter of fiscal year 2010, which ended July 31, 2009. The company reported first quarter revenue of $3.933 billion, a 6 percent increase compared to the $3.706 billion reported in the first quarter of fiscal year 2009. Revenue growth [...]

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FDA Classifies Medtronic Voluntary February Recall for Intrepid™ Intervertebral Body Fusion Device as Class II

Akillas | July 24, 2009 | 0 Comments
FDA Classifies Medtronic Voluntary February Recall for Intrepid™ Intervertebral Body Fusion Device as Class II

MINNEAPOLIS – July 23, 2009 – Medtronic, Inc. (NYSE: MDT) announced today that the U.S. Food and Drug Administration (FDA) has classified its voluntary recall action of the Intrepid™ Intervertebral Body Fusion Device as a Class II recall. Medtronic initiated a voluntary recall of the product on February 6, 2009, and communicated the risk to physicians [...]

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