
Regulation
Distalmotion receives FDA 510(k) clearance for Dexter robotic system
Distalmotion received FDA 510(k) clearance for its Dexter robotic surgery system, enabling the platform for ventral hernia repair procedures. The clearance expands the company's market access for robotic-assisted surgical applications.
The source
This brief is a MedIndexer summary of reporting by Medical Device Network. To read the full story, head to the source.
Read the full story at Medical Device Network