Last synced on 18 April 2025 at 11:05 pm

Renovis A200 PS Knee System as part of the Renovis A200 Knee System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K190122
510(k) Type
Traditional
Applicant
Renovis Surgical Technologies
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/20/2019
Days to Decision
146 days
Submission Type
Summary

Renovis A200 PS Knee System as part of the Renovis A200 Knee System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K190122
510(k) Type
Traditional
Applicant
Renovis Surgical Technologies
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/20/2019
Days to Decision
146 days
Submission Type
Summary