Brief: Aurora Receives FDA 510(K) Clearance
06/06/2022 12:22
June 6 (Reuters) - Aurora Spine Corp ASG.V :
* AURORA SPINE CORPORATION RECEIVES FDA 510(K) CLEARANCE FOR
DEXA
SOLO-LTM ANTERIOR LUMBAR INTERBODY FUSION DEVICE AS PART OF ITS
DEXA TECHNOLOGY PLATFORM
Source text for Eikon: ID:nGNXv0N0T
Further company coverage: ASG.V
((Reuters.Briefs@thomsonreuters.com;))
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