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TITANIUM RETROGRADE FEMORAL NAIL - 13 MM DIAMETER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K013923
510(k) Type
Traditional
Applicant
BIOMET ORTHOPEDICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/25/2002
Days to Decision
90 days
Submission Type
Summary

TITANIUM RETROGRADE FEMORAL NAIL - 13 MM DIAMETER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K013923
510(k) Type
Traditional
Applicant
BIOMET ORTHOPEDICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/25/2002
Days to Decision
90 days
Submission Type
Summary