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OSTEOMED EXTREMIFUSE SYSTEM

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K130412
510(k) Type
Traditional
Applicant
Osteomed
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/31/2013
Days to Decision
101 days
Submission Type
Summary

OSTEOMED EXTREMIFUSE SYSTEM

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K130412
510(k) Type
Traditional
Applicant
Osteomed
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/31/2013
Days to Decision
101 days
Submission Type
Summary