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Tenodesis Screw System

Page Type
Cleared 510(K)
510(k) Number
K183690
510(k) Type
Traditional
Applicant
Paragon 28,Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/1/2019
Days to Decision
60 days
Submission Type
Summary

Tenodesis Screw System

Page Type
Cleared 510(K)
510(k) Number
K183690
510(k) Type
Traditional
Applicant
Paragon 28,Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/1/2019
Days to Decision
60 days
Submission Type
Summary