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VITOSS BIOACTIVE FOAM BONE GRAFT SUBSTITUTE

Page Type
Cleared 510(K)
510(k) Number
K072184
510(k) Type
Traditional
Applicant
ORTHOVITA, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/18/2007
Days to Decision
43 days
Submission Type
Summary

VITOSS BIOACTIVE FOAM BONE GRAFT SUBSTITUTE

Page Type
Cleared 510(K)
510(k) Number
K072184
510(k) Type
Traditional
Applicant
ORTHOVITA, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/18/2007
Days to Decision
43 days
Submission Type
Summary