Last synced on 14 November 2025 at 11:06 pm

Arthrex Synergy Vision Imaging System

Page Type
Cleared 510(K)
510(k) Number
K251994
510(k) Type
Traditional
Applicant
Arthrex, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/16/2025
Days to Decision
111 days
Submission Type
Summary

Arthrex Synergy Vision Imaging System

Page Type
Cleared 510(K)
510(k) Number
K251994
510(k) Type
Traditional
Applicant
Arthrex, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/16/2025
Days to Decision
111 days
Submission Type
Summary