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Arthrex NanoScope System

Page Type
Cleared 510(K)
510(k) Number
K190645
510(k) Type
Traditional
Applicant
Arthrex Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/5/2019
Days to Decision
114 days
Submission Type
Summary

Arthrex NanoScope System

Page Type
Cleared 510(K)
510(k) Number
K190645
510(k) Type
Traditional
Applicant
Arthrex Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/5/2019
Days to Decision
114 days
Submission Type
Summary