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Arthrex NanoScope System

Page Type
Cleared 510(K)
510(k) Number
K201134
510(k) Type
Traditional
Applicant
Arthrex, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/4/2020
Days to Decision
129 days
Submission Type
Summary

Arthrex NanoScope System

Page Type
Cleared 510(K)
510(k) Number
K201134
510(k) Type
Traditional
Applicant
Arthrex, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/4/2020
Days to Decision
129 days
Submission Type
Summary