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ACTIFUSE FLOW BONE GRAFT SUBSTITUTE

Page Type
Cleared 510(K)
510(k) Number
K082073
510(k) Type
Traditional
Applicant
APATECH LTD.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/11/2008
Days to Decision
50 days
Submission Type
Summary

ACTIFUSE FLOW BONE GRAFT SUBSTITUTE

Page Type
Cleared 510(K)
510(k) Number
K082073
510(k) Type
Traditional
Applicant
APATECH LTD.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/11/2008
Days to Decision
50 days
Submission Type
Summary