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AGC TOTAL KNEE SYSTEM KNEE, ASCENT TOTAL KNEE SYSTEM, MAXIM COMPLETE KNEE SYSTEM, MAXIM ACCEL KNEE SYSTEM ALSO KNOWN

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K033489
510(k) Type
Traditional
Applicant
BIOMET, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/2/2004
Days to Decision
211 days
Submission Type
Summary

AGC TOTAL KNEE SYSTEM KNEE, ASCENT TOTAL KNEE SYSTEM, MAXIM COMPLETE KNEE SYSTEM, MAXIM ACCEL KNEE SYSTEM ALSO KNOWN

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K033489
510(k) Type
Traditional
Applicant
BIOMET, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/2/2004
Days to Decision
211 days
Submission Type
Summary