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Product Launch
- Ortho Kinematics Receives FDA 510(k) Clearance for KineGraph VMA System
January 20, 2012 | 09:37
ShareAUSTIN, Texas–(Healthcare Sales & Marketing Network)– Ortho Kinematics‚ a private company focused on revolutionizing spine... - Medtronic Announces Global Launch of the T2 ALTITUDE Expandable Corpectomy Device
November 15, 2011 | 10:07
ShareThe latest advancement in expandable cage technology for surgeons, hospitals and patients Join the... - Medtronic Introduces New Procedure for Minimally Invasive Spinal Fusion
November 3, 2011 | 10:08ShareMEMPHIS, Tenn.–(Healthcare Sales & Marketing Network)– Medtronic, Inc. (NYSE:MDT ) the world leader in spinal...
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Archive for Product Launch »
- Ortho Kinematics Receives FDA 510(k) Clearance for KineGraph VMA System
fda Archive
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Minutes from Negotiation Meeting on MDUFA III Reauthorization
Posted on June 22, 2011 | No CommentsShareApril 13, 2011 FDA – Industry MDUFA III Reauthorization Meeting Purpose To discuss potential financial... -
ReGen Sues FDA Seeking Restoration Of Knee-Device Approval
Posted on June 22, 2011 | No CommentsShareReGen Biologics Inc. (RGBOQ) has sued the U.S. Food and Drug Administration while seeking to... -
GAO renews critique of FDA medical device system
Posted on April 19, 2011 | No CommentsShareWASHINGTON (AP) — Government investigators say the Food and Drug Administration is putting patients at... -
FDA Issues Non-Approvable Letter for Medtronic’s Amplify
Posted on March 14, 2011 | No CommentsShareBY SANDER DUNCAN, MARCH 11, 2011 Medtronic disclosed in its 10-Q on Wednesday that the...
