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INTERPORE INDUCER BONE GRAFT DELIVERY SYRINGE

Page Type
Cleared 510(K)
510(k) Number
K972842
510(k) Type
Traditional
Applicant
Interpore Intl.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/30/1997
Days to Decision
90 days
Submission Type
Summary

INTERPORE INDUCER BONE GRAFT DELIVERY SYRINGE

Page Type
Cleared 510(K)
510(k) Number
K972842
510(k) Type
Traditional
Applicant
Interpore Intl.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/30/1997
Days to Decision
90 days
Submission Type
Summary