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Devices · Moon Surgical

Maestro System (REF100)

510(k)K242323General and Plastic SurgeryQZB

Moon Surgical is listed for Maestro System (REF100) (K242323). The FDA list gives March 14, 2025 as the date of the final decision. The lead panel is General and Plastic Surgery, and the database link on the FDA list is the 510(k) pathway. openFDA describes product code QZB as “Software Controlled Endoscope And Instrument Holder”: To hold and position endoscopes and instruments. openFDA records this submission’s decision description as “Substantially Equivalent.” This paragraph is assembled only from those public fields. It is not an FDA review, not a determination of safety or effectiveness, and not medical advice. Official record: https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfPMN/pmn.cfm?ID=K242323

Official FDA database record

Date of final decision
March 14, 2025
Company on the FDA list
Moon Surgical
Lead panel
General and Plastic Surgery
Primary product code
QZB
openFDA device name for the code
Software Controlled Endoscope And Instrument Holder
Device class
2
Regulation number
876.1500
openFDA decision description
Substantially Equivalent
openFDA decision code
SESE
Statement or summary label
Summary

Product-code text from openFDA

To hold and position endoscopes and instruments.

Other listings for this company