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BIOMET MODULAR FEMORAL REVISION SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K090757
510(k) Type
Traditional
Applicant
BIOMET, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/25/2009
Days to Decision
186 days
Submission Type
Summary

BIOMET MODULAR FEMORAL REVISION SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K090757
510(k) Type
Traditional
Applicant
BIOMET, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/25/2009
Days to Decision
186 days
Submission Type
Summary