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GENESIS II POSTERIOR STABILIZED HIGH FLEXION ARTICULAR INSERT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K032295
510(k) Type
Special
Applicant
SMITH & NEPHEW, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/21/2003
Days to Decision
27 days
Submission Type
Summary

GENESIS II POSTERIOR STABILIZED HIGH FLEXION ARTICULAR INSERT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K032295
510(k) Type
Special
Applicant
SMITH & NEPHEW, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/21/2003
Days to Decision
27 days
Submission Type
Summary