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OSTEONICS(R) 700 SERIES TOTAL KNEE MOD FEMOR COMP

Page Type
Cleared 510(K)
510(k) Number
K925372
510(k) Type
Traditional
Applicant
OSTEONICS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/12/1993
Days to Decision
112 days
Submission Type
Summary

OSTEONICS(R) 700 SERIES TOTAL KNEE MOD FEMOR COMP

Page Type
Cleared 510(K)
510(k) Number
K925372
510(k) Type
Traditional
Applicant
OSTEONICS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/12/1993
Days to Decision
112 days
Submission Type
Summary