DEN230032
- 510(k) number
- DEN230032
- Device name
- Symani Surgical System
- Applicant
- Mmi North America, Inc. FL · US
- Product code
- SAQ — Electromechanical System For Open Microsurgery
- Decision date
- 2024-04-05
- Date received
- 2023-04-25
- Decision
- Unknown
- Clearance type
- Direct
- Advisory committee
- General, Plastic Surgery
Official FDA record: DEN230032
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.