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PROFUSION BONE VOID FILLER KIT

Page Type
Cleared 510(K)
510(k) Number
K031838
510(k) Type
Traditional
Applicant
BIOGENERATION
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/30/2003
Days to Decision
136 days
Submission Type
Summary

PROFUSION BONE VOID FILLER KIT

Page Type
Cleared 510(K)
510(k) Number
K031838
510(k) Type
Traditional
Applicant
BIOGENERATION
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/30/2003
Days to Decision
136 days
Submission Type
Summary