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ArthrexVIP Web Portal

Page Type
Cleared 510(K)
510(k) Number
K193523
510(k) Type
Special
Applicant
Arthrex, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/30/2020
Days to Decision
133 days
Submission Type
Summary

ArthrexVIP Web Portal

Page Type
Cleared 510(K)
510(k) Number
K193523
510(k) Type
Special
Applicant
Arthrex, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/30/2020
Days to Decision
133 days
Submission Type
Summary