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PRO OSTEON IMPLANT 500R RESORBABLE BONE GRAFT SUBSTITUTE

Page Type
Cleared 510(K)
510(k) Number
K990131
510(k) Type
Traditional
Applicant
INTERPORE CROSS INTL.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/2/1999
Days to Decision
47 days
Submission Type
Summary

PRO OSTEON IMPLANT 500R RESORBABLE BONE GRAFT SUBSTITUTE

Page Type
Cleared 510(K)
510(k) Number
K990131
510(k) Type
Traditional
Applicant
INTERPORE CROSS INTL.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/2/1999
Days to Decision
47 days
Submission Type
Summary