DEN230084

Dexter L6 System

510(k) number
DEN230084
Device name
Dexter L6 System
Applicant
Distalmotion SA CH
Product code
SDD — Electromechanical Surgical System Wherein The Surgeo
Decision date
2024-10-25
Date received
2023-12-15
Decision
Unknown
Clearance type
Direct
Advisory committee
General, Plastic Surgery
Official FDA record: DEN230084
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.