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GENESIS II POROUS PLUS HA KNEE SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K032683
510(k) Type
Abbreviated
Applicant
SMITH & NEPHEW, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/15/2003
Days to Decision
47 days
Submission Type
Summary

GENESIS II POROUS PLUS HA KNEE SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K032683
510(k) Type
Abbreviated
Applicant
SMITH & NEPHEW, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/15/2003
Days to Decision
47 days
Submission Type
Summary