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BIODRIVE CANNULATED SCREW SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K082874
510(k) Type
Traditional
Applicant
BIOMET TRAUMA
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/5/2009
Days to Decision
129 days
Submission Type
Summary

BIODRIVE CANNULATED SCREW SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K082874
510(k) Type
Traditional
Applicant
BIOMET TRAUMA
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/5/2009
Days to Decision
129 days
Submission Type
Summary