Last synced on 14 November 2025 at 11:06 pm

DURACON MONOLITHIC STABILIZER FEMORAL COMPONENT

Page Type
Cleared 510(K)
510(k) Number
K954138
510(k) Type
Traditional
Applicant
HOWMEDICA CORP.
Country
United States
FDA Decision
Substantially Equivalent for Some Indications
Decision Date
11/21/1995
Days to Decision
81 days
Submission Type
Summary

DURACON MONOLITHIC STABILIZER FEMORAL COMPONENT

Page Type
Cleared 510(K)
510(k) Number
K954138
510(k) Type
Traditional
Applicant
HOWMEDICA CORP.
Country
United States
FDA Decision
Substantially Equivalent for Some Indications
Decision Date
11/21/1995
Days to Decision
81 days
Submission Type
Summary