The clearance of the expanded indications is based on extensive data from a variety of studies and sources showing that it is safe and effective to use silicon nitride devices in multi-level procedures.
“We are very pleased to become the first company to receive FDA clearance for multi-level cervical interbody cage indications,” said Sonny Bal, MD, chairman and CEO of Amedica.
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K2M sets follow-on offering at $18.75 per share — 5 things to know
Implanet’s JAZZ technology receives intellectual patent protection in Europe
FTC makes second request for additional information on Wright Medical-Tornier merger — 5 points
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