K233550 is an FDA 510(k) clearance for the MOSAIC 3D (Surgical Laser), a Powered Laser Surgical Instrument With Microbeamfractional Output (Class II — Special Controls, product code ONG), submitted by Lutronic Aesthetic (Billerica, US). The FDA issued a Cleared decision on January 2, 2024, 60 days after receiving the submission on November 3, 2023. This device falls under the General & Plastic Surgery review panel. Regulated under 21 CFR 878.4810.
| 510(k) Number | K233550 FDA.gov |
| FDA Decision | Cleared SESE |
| Date Received | November 03, 2023 |
| Decision Date | January 02, 2024 |
| Days to Decision | 60 days |
| Submission Type | Traditional |
| Review Panel | General & Plastic Surgery (SU) |
| Summary | Summary PDF |
| Product Code | ONG — Powered Laser Surgical Instrument With Microbeamfractional Output |
| Device Class | Class II — Special Controls |
| CFR Regulation | 21 CFR 878.4810 |
| Definition | A Laser (light Amplification By Stimulated Emission Of Radiation) Based Device Having Coherence, Collimated And Typically Monochromatic Radiation. The Laser Output Is In Form Of Tiny Beams In Micro Range. Typically, Indicated To Be Used In Medical Specialties Of General And Plastic Surgery And Of Dermatology/aesthetic To Destroy, Remove Or Coagulate Tissue, Generally Soft Tissue. Indication For Use Can Be General And/or Specific. The Classification Regulation 21 Cfr 878.4810 Describes A Device That Is Carbon Dioxide Or Argon Laser Intended To Cut, Destroy, Remove Or Coagulate Tissue By The Light. |