510(k) K201837
K201837 is an FDA 510(k) premarket notification submitted by Neotract, Inc. for the device "UroLift 2 System (formerly UL500), UroLift 2 Delivery Handle, UroLift 2 Implant Cartridge". The FDA issued a decision of Substantially Equivalent on July 31, 2020. The device falls under product code PEW (Implantable Transprostatic Tissue Retractor System), a Class II device regulated under 21 CFR 876.5530. Neotract, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- July 31, 2020
- Date Received
- July 2, 2020
- Clearance Type
- Special
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Implantable Transprostatic Tissue Retractor System
- Device Class
- Class II
- Regulation Number
- 876.5530
- Review Panel
- GU
- Submission Type
The treatment of symptoms due to urinary outflow obstruction secondary to benign prostatic hyperplasia (BPH) in men age 50 and above.