Last synced on 25 January 2026 at 3:41 am

AOS Clavicle Intramedullary Device

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K143204
510(k) Type
Traditional
Applicant
Advanced Orthopaedic Solutions, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/3/2015
Days to Decision
208 days
Submission Type
Summary

AOS Clavicle Intramedullary Device

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K143204
510(k) Type
Traditional
Applicant
Advanced Orthopaedic Solutions, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/3/2015
Days to Decision
208 days
Submission Type
Summary