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VITOSS BIOACTIVE FOAM BONE GRAFT SUBSTITUTE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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