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DUOWEDGE SYNTHETIC BONE SUBSTITUTE

Page Type
Cleared 510(K)
510(k) Number
K073214
510(k) Type
Traditional
Applicant
KASIOS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/1/2009
Days to Decision
748 days
Submission Type
Summary

DUOWEDGE SYNTHETIC BONE SUBSTITUTE

Page Type
Cleared 510(K)
510(k) Number
K073214
510(k) Type
Traditional
Applicant
KASIOS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/1/2009
Days to Decision
748 days
Submission Type
Summary