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KINEMAX TIBIAL STEM EXTENSION

Page Type
Cleared 510(K)
510(k) Number
K896452
510(k) Type
Traditional
Applicant
HOWMEDICA CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/4/1990
Days to Decision
56 days

KINEMAX TIBIAL STEM EXTENSION

Page Type
Cleared 510(K)
510(k) Number
K896452
510(k) Type
Traditional
Applicant
HOWMEDICA CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/4/1990
Days to Decision
56 days