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COMPRESS DISTAL FEMORAL REPLACEMENT SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K041352
510(k) Type
Traditional
Applicant
BIOMET, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/30/2004
Days to Decision
71 days
Submission Type
Summary

COMPRESS DISTAL FEMORAL REPLACEMENT SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K041352
510(k) Type
Traditional
Applicant
BIOMET, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/30/2004
Days to Decision
71 days
Submission Type
Summary