K240200 is an FDA 510(k) clearance for the HYDROS Robotic System. This device is classified as a Fluid Jet Removal System (Class II - Special Controls, product code PZP).
Submitted by Procept Biorobotics (San Jose, US). The FDA issued a Cleared decision on August 20, 2024, 208 days after receiving the submission on January 25, 2024.
This device falls under the Gastroenterology & Urology FDA review panel. Regulated under 21 CFR 876.4350. The System Is Used For Removal Of Prostate Tissue With A Fluid Jet..
| 510(k) Number | K240200 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | January 25, 2024 |
| Decision Date | August 20, 2024 |
| Days to Decision | 208 days |
| Submission Type | Traditional |
| Review Panel | Gastroenterology & Urology (GU) |
| Summary | Summary PDF |
| Product Code | PZP - Fluid Jet Removal System |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 876.4350 |
| Definition | The System Is Used For Removal Of Prostate Tissue With A Fluid Jet. |