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Arthrex SwiveLock

Page Type
Cleared 510(K)
510(k) Number
K173845
510(k) Type
Traditional
Applicant
Arthrex Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/6/2018
Days to Decision
230 days
Submission Type
Summary

Arthrex SwiveLock

Page Type
Cleared 510(K)
510(k) Number
K173845
510(k) Type
Traditional
Applicant
Arthrex Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/6/2018
Days to Decision
230 days
Submission Type
Summary