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Medical Device

Biomet Submits New 510(k) For Signature, Reports Disappointing Q1

This article was originally published in The Gray Sheet

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Executive Summary

Biomet has submitted a new 510(k) for its Signature personalized knee surgery instrumentation system to help resolve a July 27 FDA warning letter, according to CEO Jeffrey Binder.

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This copy is for your personal, non-commercial use. For high-quality copies or electronic reprints for distribution to colleagues or customers, please call +44 (0) 20 3377 3183

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