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Injection Screw

Page Type
Cleared 510(K)
510(k) Number
K173556
510(k) Type
Traditional
Applicant
Biedermann Medtech, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/13/2018
Days to Decision
238 days
Submission Type
Summary

Injection Screw

Page Type
Cleared 510(K)
510(k) Number
K173556
510(k) Type
Traditional
Applicant
Biedermann Medtech, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/13/2018
Days to Decision
238 days
Submission Type
Summary