K242251
- 510(k) number
- K242251
- Device name
- Litho 60; Litho 100; Litho 150
- Applicant
- Quanta System Spa IT
- Product code
- GEX — Powered Laser Surgical Instrument
- Decision date
- 2024-09-03
- Date received
- 2024-07-31
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Advisory committee
- General, Plastic Surgery
510(k) Summary (official FDA PDF): K242251.pdf
Official FDA record: K242251
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.