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Cannulated Screw

Page Type
Cleared 510(K)
510(k) Number
K161058
510(k) Type
Traditional
Applicant
MIAMI DEVICE SOLUTIONS, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/29/2016
Days to Decision
105 days
Submission Type
Summary

Cannulated Screw

Page Type
Cleared 510(K)
510(k) Number
K161058
510(k) Type
Traditional
Applicant
MIAMI DEVICE SOLUTIONS, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/29/2016
Days to Decision
105 days
Submission Type
Summary