Last synced on 14 November 2025 at 11:06 pm

Epic Extremity Cannulated Screw System

Page Type
Cleared 510(K)
510(k) Number
K153333
510(k) Type
Traditional
Applicant
Epic Extremity, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/19/2016
Days to Decision
61 days
Submission Type
Summary

Epic Extremity Cannulated Screw System

Page Type
Cleared 510(K)
510(k) Number
K153333
510(k) Type
Traditional
Applicant
Epic Extremity, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/19/2016
Days to Decision
61 days
Submission Type
Summary