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LOWER EXTREMITY EXTERNAL FIXATION - EXPANDED INDICATIONS

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K081244
510(k) Type
Traditional
Applicant
BIOMET TRAUMA
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/30/2008
Days to Decision
90 days
Submission Type
Summary

LOWER EXTREMITY EXTERNAL FIXATION - EXPANDED INDICATIONS

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K081244
510(k) Type
Traditional
Applicant
BIOMET TRAUMA
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/30/2008
Days to Decision
90 days
Submission Type
Summary