510(k) K240598

Maestro System (REF100) by Moon Surgical — Product Code FQO

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
June 3, 2024
Date Received
March 4, 2024
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Table, Operating-Room, Ac-Powered
Device Class
Class I
Regulation Number
878.4960
Review Panel
SU
Submission Type