この記事の翻訳を準備しています。それまでの間、英語の原文を表示します。
ビジネス · 2007/3/281 分で読めます
Determination of Regulatory Review Period for Purposes of Patent Extension; INFUSE BONE GRAFT/LT-CAGE LUMBAR TAPERED FUSION DEVICE
ローカル自動翻訳 · 情報源の原言語
概要
The Food and Drug Administration (FDA) has determined the regulatory review period for INFUSE BONE GRAFT/LT-CAGE LUMBAR TAPERED FUSION DEVICE and is publishing this notice of that determination as required by law. FDA has made the determination because of the submission of two applications to the Director of Patents and Trademarks, Department of Commerce, for the extension of patents which claim that medical device.
情報源の原言語: Federal Register — Food and Drug Administration原文の発表を開く →