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7000 SERIES MODULAR TIBIAL COMPONENTS

Page Type
Cleared 510(K)
510(k) Number
K915192
510(k) Type
Traditional
Applicant
OSTEONICS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/14/1992
Days to Decision
87 days
Submission Type
Statement

7000 SERIES MODULAR TIBIAL COMPONENTS

Page Type
Cleared 510(K)
510(k) Number
K915192
510(k) Type
Traditional
Applicant
OSTEONICS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/14/1992
Days to Decision
87 days
Submission Type
Statement