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REGENEREX PATELLA COMPONENTS

Page Type
Cleared 510(K)
510(k) Number
K083782
510(k) Type
Traditional
Applicant
BIOMET MANUFACTURING CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/3/2009
Days to Decision
105 days
Submission Type
Summary

REGENEREX PATELLA COMPONENTS

Page Type
Cleared 510(K)
510(k) Number
K083782
510(k) Type
Traditional
Applicant
BIOMET MANUFACTURING CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/3/2009
Days to Decision
105 days
Submission Type
Summary