Last synced on 14 November 2025 at 11:06 pm

AFX Femoral Implant with Inserter

Page Type
Cleared 510(K)
510(k) Number
K192428
510(k) Type
Special
Applicant
Cayenne Medical
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/5/2019
Days to Decision
30 days
Submission Type
Summary

AFX Femoral Implant with Inserter

Page Type
Cleared 510(K)
510(k) Number
K192428
510(k) Type
Special
Applicant
Cayenne Medical
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/5/2019
Days to Decision
30 days
Submission Type
Summary