Last synced on 18 April 2025 at 11:05 pm

Arthrx Fracture Plates

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K213837
510(k) Type
Traditional
Applicant
Arthrex Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/2/2022
Days to Decision
144 days
Submission Type
Summary

Arthrx Fracture Plates

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K213837
510(k) Type
Traditional
Applicant
Arthrex Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/2/2022
Days to Decision
144 days
Submission Type
Summary