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COMPRESS DISTAL FEMORAL REPLACEMENT

Page Type
Cleared 510(K)
510(k) Number
K031804
510(k) Type
Traditional
Applicant
BIOMET, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/18/2003
Days to Decision
190 days
Submission Type
Summary

COMPRESS DISTAL FEMORAL REPLACEMENT

Page Type
Cleared 510(K)
510(k) Number
K031804
510(k) Type
Traditional
Applicant
BIOMET, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/18/2003
Days to Decision
190 days
Submission Type
Summary