Last synced on 14 November 2025 at 11:06 pm

Arthrex NanoScope System

Page Type
Cleared 510(K)
510(k) Number
K243008
510(k) Type
Traditional
Applicant
Arthrex, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/22/2025
Days to Decision
118 days
Submission Type
Summary

Arthrex NanoScope System

Page Type
Cleared 510(K)
510(k) Number
K243008
510(k) Type
Traditional
Applicant
Arthrex, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/22/2025
Days to Decision
118 days
Submission Type
Summary