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DURACON STABILIZER FEMORAL COMPONENT AND INSERT

Page Type
Cleared 510(K)
510(k) Number
K932070
510(k) Type
Traditional
Applicant
HOWMEDICA CORP.
Country
United States
FDA Decision
Substantially Equivalent for Some Indications
Decision Date
3/22/1995
Days to Decision
693 days
Submission Type
Summary

DURACON STABILIZER FEMORAL COMPONENT AND INSERT

Page Type
Cleared 510(K)
510(k) Number
K932070
510(k) Type
Traditional
Applicant
HOWMEDICA CORP.
Country
United States
FDA Decision
Substantially Equivalent for Some Indications
Decision Date
3/22/1995
Days to Decision
693 days
Submission Type
Summary