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CORTOSS BONE AUGMENTATION MATERIAL

Page Type
Cleared 510(K)
510(k) Number
K080108
510(k) Type
Traditional
Applicant
Orthovita, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/5/2009
Days to Decision
507 days
Submission Type
Summary

CORTOSS BONE AUGMENTATION MATERIAL

Page Type
Cleared 510(K)
510(k) Number
K080108
510(k) Type
Traditional
Applicant
Orthovita, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/5/2009
Days to Decision
507 days
Submission Type
Summary