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PRELUDE PF FEMORAL COMPONENTS (MIM COCRMO), PRELUDE PF FEMORAL COMPONENTS (CAST COCRMO), PRELUDE PF PATELLA COMPONENTS,

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K123907
510(k) Type
Traditional
Applicant
BIOMET MANUFACTURING CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/3/2013
Days to Decision
258 days
Submission Type
Summary

PRELUDE PF FEMORAL COMPONENTS (MIM COCRMO), PRELUDE PF FEMORAL COMPONENTS (CAST COCRMO), PRELUDE PF PATELLA COMPONENTS,

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K123907
510(k) Type
Traditional
Applicant
BIOMET MANUFACTURING CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/3/2013
Days to Decision
258 days
Submission Type
Summary