Last synced on 14 November 2025 at 11:06 pm

TriMAX Implant System

Page Type
Cleared 510(K)
510(k) Number
K190722
510(k) Type
Traditional
Applicant
CrossRoads Extemity Systems, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/16/2019
Days to Decision
149 days
Submission Type
Summary

TriMAX Implant System

Page Type
Cleared 510(K)
510(k) Number
K190722
510(k) Type
Traditional
Applicant
CrossRoads Extemity Systems, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/16/2019
Days to Decision
149 days
Submission Type
Summary