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TITANIUM REPICCI II UNICONDYLAR FEMORAL KNEE COMPONENTS COCR REPICCI II UNICONDYLAR KNEE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K063515
510(k) Type
Traditional
Applicant
BIOMET MANUFACTURING, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/2/2007
Days to Decision
73 days
Submission Type
Summary

TITANIUM REPICCI II UNICONDYLAR FEMORAL KNEE COMPONENTS COCR REPICCI II UNICONDYLAR KNEE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K063515
510(k) Type
Traditional
Applicant
BIOMET MANUFACTURING, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/2/2007
Days to Decision
73 days
Submission Type
Summary