Biomet’s OsseoTi Porous shell receives regulatory clearance; successfully implanted

Biomet announced regulatory clearance and the first clinical use of OsseoTi Porous Technology for total hip arthroplasty.

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The G7 OsseoTi shell received the CE mark and FDA clearance in November and December 2014, respectively. The first clinical use of the technology also took place in December 2014.

 

The G7 OsseoTi shell is used in conjunction with Biomet’s G7 Acetabular System, a multi-bearing acetabular platform designed for primary and revision hip arthroplasty.

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