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DURACON POSTERIOR FEMORAL SPACER

Page Type
Cleared 510(K)
510(k) Number
K963242
510(k) Type
Traditional
Applicant
HOWMEDICA CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/14/1996
Days to Decision
87 days
Submission Type
Summary

DURACON POSTERIOR FEMORAL SPACER

Page Type
Cleared 510(K)
510(k) Number
K963242
510(k) Type
Traditional
Applicant
HOWMEDICA CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/14/1996
Days to Decision
87 days
Submission Type
Summary