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FIBERGRAFT AERIDYAN Matrix Bone Graft Substitute

Page Type
Cleared 510(K)
510(k) Number
K182670
510(k) Type
Traditional
Applicant
Prosidyan, Inc
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/20/2018
Days to Decision
86 days
Submission Type
Summary

FIBERGRAFT AERIDYAN Matrix Bone Graft Substitute

Page Type
Cleared 510(K)
510(k) Number
K182670
510(k) Type
Traditional
Applicant
Prosidyan, Inc
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/20/2018
Days to Decision
86 days
Submission Type
Summary