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BRIEF-NuVasive receives expanded FDA 510(k) clearance For TLX Interbody System used in TLIF procedures
2017年10月16日 / 下午12点47分 / 1 个月前

BRIEF-NuVasive receives expanded FDA 510(k) clearance For TLX Interbody System used in TLIF procedures

Oct 16 (Reuters) - Nuvasive Inc

* NuVasive receives expanded FDA 510(k) clearance For TLX Interbody System used in TLIF procedures

* Says ‍new clearance introduces an expandable 20 degree cage and broader indications for use​ Source text for Eikon: Further company coverage:

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