Last synced on 14 November 2025 at 11:06 pm

Arthrex Shoulder System

Page Type
Cleared 510(K)
510(k) Number
K171841
510(k) Type
Traditional
Applicant
Arthrex Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/29/2018
Days to Decision
282 days
Submission Type
Summary

Arthrex Shoulder System

Page Type
Cleared 510(K)
510(k) Number
K171841
510(k) Type
Traditional
Applicant
Arthrex Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/29/2018
Days to Decision
282 days
Submission Type
Summary