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OSTEONICS SERIES 7000 TOTAL KNEE AUGMENTED FEMORAL COMPONENT

Page Type
Cleared 510(K)
510(k) Number
K973406
510(k) Type
Traditional
Applicant
OSTEONICS CORP.
Country
United States
FDA Decision
Substantially Equivalent for Some Indications
Decision Date
12/8/1997
Days to Decision
90 days

OSTEONICS SERIES 7000 TOTAL KNEE AUGMENTED FEMORAL COMPONENT

Page Type
Cleared 510(K)
510(k) Number
K973406
510(k) Type
Traditional
Applicant
OSTEONICS CORP.
Country
United States
FDA Decision
Substantially Equivalent for Some Indications
Decision Date
12/8/1997
Days to Decision
90 days