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OSTEONICS 7000 SERIES TOTAL KNEE TIBIAL COMPONENTS

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K910990
510(k) Type
Traditional
Applicant
OSTEONICS CORP.
Country
United States
FDA Decision
Substantially Equivalent for Some Indications
Decision Date
6/19/1991
Days to Decision
104 days

OSTEONICS 7000 SERIES TOTAL KNEE TIBIAL COMPONENTS

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K910990
510(k) Type
Traditional
Applicant
OSTEONICS CORP.
Country
United States
FDA Decision
Substantially Equivalent for Some Indications
Decision Date
6/19/1991
Days to Decision
104 days