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Extremity Medical Receives FDA Clearance for New Hammertoe Anchor Implant Made of Solvay's ...

2014-06-11 06:00:00| Industrial Newsroom - All News for Today

Industry's First PEEK Hammertoe Fusion Device Boasts Unique Design to Ensure Stability and Maintenance<br /> <br /> ROSEMONT, Ill. &ndash; Extremity Medical LLC, Parsippany, N.J., an entrepreneurial-based manufacturer of orthopedic implants for the distal extremities, has received 510(k) clearance from the U.S. Food Drug Administration (FDA) for its new HammerFiX&trade; IP fusion system made of Zeniva® polyetheretherketone (PEEK) resin from Solvay Specialty Polymers. Zeniva® PEEK &ndash; part ...This story is related to the following:Chemical Processing and Waste ManagementSearch for suppliers of: Biomaterials |

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FDA Removes Clinical Hold on Study of Pancreatic Cancer Drug

2014-06-08 05:12:05| Biotech - Topix.net

The FDA has removed its clinical hold on patient enrollment and dosing of PEGPH20 in an ongoing phase II trial evaluating the investigational compound in patients with pancreatic cancer, permitting the study to resume under a revised protocol.

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UPDATE 1-U.S. FDA approves Biogen's hemophilia A drug Eloctate

2014-06-07 02:45:29| Appliances - Topix.net

The U.S. Food and Drug Administration said on Friday it approved Biogen Idec Inc's long-lasting hemophilia A drug, Eloctate, adding another product to the company's nascent portfolio of drugs for non-malignant blood disorders.

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NPA Taps Former FDA Chief

2014-06-03 17:30:00| Happi Breaking News

Supplement regulation implementation expert Hilmas joins team.

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FDA OKs Generic Versions of Pain Pill Celebrex

2014-05-31 00:25:55| Biotech - Topix.net

The FDA approved low-cost versions from generic drugmakers Teva Pharmaceutical Industries Limited and Mylan Inc. Teva has exclusive marketing rights to three doses of the drug for 180 days.

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