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MIMIX BONE REPLACEMENT SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K003494
510(k) Type
Traditional
Applicant
BIOMET, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/9/2001
Days to Decision
147 days
Submission Type
Summary

MIMIX BONE REPLACEMENT SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K003494
510(k) Type
Traditional
Applicant
BIOMET, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/9/2001
Days to Decision
147 days
Submission Type
Summary