The following data is part of a premarket notification filed by Neotract, Inc. with the FDA for Urolift System (ul500).
| Device ID | K172359 |
| 510k Number | K172359 |
| Device Name: | UroLift System (UL500) |
| Classification | Implantable Transprostatic Tissue Retractor System |
| Applicant | NeoTract, Inc. 4473 Willow Road Suite 100 Pleasanton, CA 94588 |
| Contact | Louis-pierre Marcoux |
| Correspondent | Louis-pierre Marcoux NeoTract, Inc. 4473 Willow Road Suite 100 Pleasanton, CA 94588 |
| Product Code | PEW |
| CFR Regulation Number | 876.5530 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Special |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2017-08-04 |
| Decision Date | 2017-08-18 |
| Summary: | summary |