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OSTEOMED HEADLESS CANNULATED SCREW SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K063298
510(k) Type
Traditional
Applicant
OSTEOMED L.P.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/2/2007
Days to Decision
121 days
Submission Type
Summary

OSTEOMED HEADLESS CANNULATED SCREW SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K063298
510(k) Type
Traditional
Applicant
OSTEOMED L.P.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/2/2007
Days to Decision
121 days
Submission Type
Summary