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TIBIAL & PATELLAR COMPONENTS FOR THE PROFIX & GENESIS II TOTAL KNEE SYSTEMS

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K002740
510(k) Type
Abbreviated
Applicant
SMITH & NEPHEW, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/30/2000
Days to Decision
90 days
Submission Type
Summary

TIBIAL & PATELLAR COMPONENTS FOR THE PROFIX & GENESIS II TOTAL KNEE SYSTEMS

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K002740
510(k) Type
Abbreviated
Applicant
SMITH & NEPHEW, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/30/2000
Days to Decision
90 days
Submission Type
Summary