K240598
- 510(k) number
- K240598
- Device name
- Maestro System (REF100)
- Applicant
- Moon Surgical FR
- Product code
- FQO — Table, Operating-Room, Ac-Powered
- Decision date
- 2024-06-03
- Date received
- 2024-03-04
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- General, Plastic Surgery
PDFDownload 510(k) SummaryArchived here · 0.6 MB · U.S. public domain
Also available from FDA: K240598.pdf
Official FDA record: K240598
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.