FDAnews Device Daily Bulletin

OSTEOTECH RECEIVES ITS FIRST GRAFTON DMB 510(K) FDA CLEARANCE

Dec. 1, 2005
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Osteotech, Inc. announced today that the Food and Drug Administration ("FDA") has cleared its 510(k) for Grafton Plus DBM Paste for use as a bone graft extender, bone graft substitute and bone void filler in orthopedic procedures.

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