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REGENEREX ULTRA POROUS CONSTRUCT-FEMORAL AND TIBIAL KNEE AUGMENTS

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K053505
510(k) Type
Traditional
Applicant
BIOMET MANUFACTURING, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/14/2006
Days to Decision
241 days
Submission Type
Summary

REGENEREX ULTRA POROUS CONSTRUCT-FEMORAL AND TIBIAL KNEE AUGMENTS

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K053505
510(k) Type
Traditional
Applicant
BIOMET MANUFACTURING, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/14/2006
Days to Decision
241 days
Submission Type
Summary