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BIOMET PRE-CALIBRATED COMPUTER AIDED SURGERY NAVIGATION INSTRUMENTS FOR HIP APPLICATIONS

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K060121
510(k) Type
Traditional
Applicant
BIOMET MANUFACTURING CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/21/2006
Days to Decision
63 days
Submission Type
Summary

BIOMET PRE-CALIBRATED COMPUTER AIDED SURGERY NAVIGATION INSTRUMENTS FOR HIP APPLICATIONS

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K060121
510(k) Type
Traditional
Applicant
BIOMET MANUFACTURING CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/21/2006
Days to Decision
63 days
Submission Type
Summary