Clearance Summary
iSR`obot Mona Lisa 2.0 received FDA 510(k) clearance under submission number K232320, sponsored by Biobot Surgical Pte., Ltd.. The device was reviewed via the Special premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 2023-12-21.
- Submission: K232320
- Applicant / Sponsor: Biobot Surgical Pte., Ltd.
- Clearance pathway: Special
- Review panel: Radiology
- Device class: Class II
- Regulation citation: 21 CFR 892.1560
- Decision date: 2023-12-21
Classification & Regulation
This clearance is catalogued under FDA product code IYO and 21 CFR 892.1560, within the Radiology review panel as a Class II device.