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CANNULATED ARTHRORIVET AND CANNULATED RC ARTHRORIVET

Page Type
Cleared 510(K)
510(k) Number
K033519
510(k) Type
Special
Applicant
BIOMET, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/5/2003
Days to Decision
28 days
Submission Type
Summary

CANNULATED ARTHRORIVET AND CANNULATED RC ARTHRORIVET

Page Type
Cleared 510(K)
510(k) Number
K033519
510(k) Type
Special
Applicant
BIOMET, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/5/2003
Days to Decision
28 days
Submission Type
Summary