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DURACON MODULAR FEMORAL COMPONENT AND FEMORAL SPAC

Page Type
Cleared 510(K)
510(k) Number
K920034
510(k) Type
Traditional
Applicant
PFIZER HOSPITAL PRODUCTS GROUP, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/18/1992
Days to Decision
72 days
Submission Type
Statement

DURACON MODULAR FEMORAL COMPONENT AND FEMORAL SPAC

Page Type
Cleared 510(K)
510(k) Number
K920034
510(k) Type
Traditional
Applicant
PFIZER HOSPITAL PRODUCTS GROUP, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/18/1992
Days to Decision
72 days
Submission Type
Statement