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IMBIBE II SYRINGE

Page Type
Cleared 510(K)
510(k) Number
K030208
510(k) Type
Traditional
Applicant
ORTHOVITA, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/16/2003
Days to Decision
85 days
Submission Type
Summary

IMBIBE II SYRINGE

Page Type
Cleared 510(K)
510(k) Number
K030208
510(k) Type
Traditional
Applicant
ORTHOVITA, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/16/2003
Days to Decision
85 days
Submission Type
Summary