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FIBERGRAFT Aeridyan Matrix Bone Graft Substitute

Page Type
Cleared 510(K)
510(k) Number
K213803
510(k) Type
Traditional
Applicant
Prosidyan, Inc
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/23/2022
Days to Decision
260 days
Submission Type
Summary

FIBERGRAFT Aeridyan Matrix Bone Graft Substitute

Page Type
Cleared 510(K)
510(k) Number
K213803
510(k) Type
Traditional
Applicant
Prosidyan, Inc
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/23/2022
Days to Decision
260 days
Submission Type
Summary