Brief: Nuvasive Inc - Received 510(K) Clearance From FDA For Use Of Its Modulus Cervical Interbody Implant With A Bone Void Filler

NuVasive

21/02/2023 12:07

Feb 21 (Reuters) - NuVasive Inc  NUVA.O :
    * NUVASIVE INC - RECEIVED 510(K) CLEARANCE FROM FDA FOR USE
OF ITS
MODULUS CERVICAL INTERBODY IMPLANT WITH A BONE VOID FILLER

Source text for Eikon:  ID:nPnc313R5a 
Further company coverage:  NUVA.O 
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