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VITOSS BIOACTIVE FOAM PACK BONE GRAFT SUBSTITUTE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K081439
510(k) Type
Special
Applicant
ORTHOVITA, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/17/2008
Days to Decision
26 days
Submission Type
Summary

VITOSS BIOACTIVE FOAM PACK BONE GRAFT SUBSTITUTE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K081439
510(k) Type
Special
Applicant
ORTHOVITA, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/17/2008
Days to Decision
26 days
Submission Type
Summary