Last synced on 25 January 2026 at 3:41 am

Arthrex Compression FT Pins

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K220839
510(k) Type
Traditional
Applicant
Arthrex, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/19/2022
Days to Decision
180 days
Submission Type
Summary

Arthrex Compression FT Pins

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K220839
510(k) Type
Traditional
Applicant
Arthrex, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/19/2022
Days to Decision
180 days
Submission Type
Summary