Last synced on 25 January 2026 at 3:41 am

OSS/Arcos IM Total Femur Rod

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K152621
510(k) Type
Special
Applicant
Biomet, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/14/2015
Days to Decision
30 days
Submission Type
Summary

OSS/Arcos IM Total Femur Rod

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K152621
510(k) Type
Special
Applicant
Biomet, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/14/2015
Days to Decision
30 days
Submission Type
Summary