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OSTEOMED EXTREMIFUSE SYSTEM

Page Type
Cleared 510(K)
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)
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