Last synced on 14 November 2025 at 11:06 pm

RenaNav Ureteroscope System

Page Type
Cleared 510(K)
510(k) Number
K223097
510(k) Type
Traditional
Applicant
CenterPoint Systems LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/31/2023
Days to Decision
304 days
Submission Type
Summary

RenaNav Ureteroscope System

Page Type
Cleared 510(K)
510(k) Number
K223097
510(k) Type
Traditional
Applicant
CenterPoint Systems LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/31/2023
Days to Decision
304 days
Submission Type
Summary