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VITOMATRIX

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K091618
510(k) Type
Traditional
Applicant
Orthovita, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/27/2010
Days to Decision
481 days
Submission Type
Summary

VITOMATRIX

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K091618
510(k) Type
Traditional
Applicant
Orthovita, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/27/2010
Days to Decision
481 days
Submission Type
Summary