K221306 is an FDA 510(k) clearance for the SOLTIVE Pro SuperPulsed Laser, SOLTIVE Premium SuperPulsed Laser, SOLTIVE SuperPulsed Laser Fibers, and Accessories, a Powered Laser Surgical Instrument (Class II — Special Controls, product code GEX), submitted by Gyrus Acmi, Inc. (Westborough, US). The FDA issued a Cleared decision on January 27, 2023, 267 days after receiving the submission on May 5, 2022. This device falls under the Gastroenterology & Urology review panel. Regulated under 21 CFR 878.4810.
| 510(k) Number | K221306 FDA.gov |
| FDA Decision | Cleared SESE |
| Date Received | May 05, 2022 |
| Decision Date | January 27, 2023 |
| Days to Decision | 267 days |
| Submission Type | Traditional |
| Review Panel | Gastroenterology & Urology (GU) |
| Summary | Summary PDF |
| Product Code | GEX — Powered Laser Surgical Instrument |
| 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. Typically Indicated To To Cut, Destroy, Remove Or Coagulate Tissue, Generally Soft Tissue, For General Surgical Purpose In Medical Specialties Of General And Plastic Surgery, Dermatology/aesthetic, Podiatry, Otolaryngology (ent), Gynecology, Neurosurgery, Orthopedics (soft Tissue), Dental And Oral Surgery, And Dentistry. 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. |