Aurora Spine Corporation Receives FDA 510(k) Clearance for DEXA SOLO-LTM Anterior Lumbar Interbody Fusion Device as part of its DEXA Technology Platform.
In: Marketwired, 2022-06-06
Zeitungsartikel
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Aurora Spine Corporation Receives FDA 510(k) Clearance for DEXA SOLO-LTM Anterior Lumbar Interbody Fusion Device as part of its DEXA Technology Platform.
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Zeitschrift: | Marketwired, 2022-06-06 |
Veröffentlichung: | 2022 |
Medientyp: | Zeitungsartikel |
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