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GENESIS II ZIRCONIUM FEMORAL COMPONENT/PROFIX ZIRCONIUM FEMORAL COMPONENT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K962557
510(k) Type
Traditional
Applicant
SMITH & NEPHEW RICHARDS, INC.
Country
United States
FDA Decision
Substantially Equivalent for Some Indications
Decision Date
12/5/1996
Days to Decision
157 days

GENESIS II ZIRCONIUM FEMORAL COMPONENT/PROFIX ZIRCONIUM FEMORAL COMPONENT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K962557
510(k) Type
Traditional
Applicant
SMITH & NEPHEW RICHARDS, INC.
Country
United States
FDA Decision
Substantially Equivalent for Some Indications
Decision Date
12/5/1996
Days to Decision
157 days